Recalls in Missouri (page 34)
3996 recalls.
- TheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
Consumer productReported February 27, 2026 · The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal... - TheKiddoSpace Recalls Reusable Water Balloons Due to Risk of Injury from Phthalate Exposure; Violate Federal Phthalates Ban
Consumer productReported February 27, 2026 · The cord lock on the recalled water ballons' storage bags contain a regulated phthalate, which violate the federal phthalate ban. Phthalates are toxic if... - TheKiddoSpace Recalls Children's Fingerpainting Kits Due to Risk of Injury from Hazardous Substances and Phthalate Exposure; Violates Federal Hazardous Substances Act and Phthalates Ban
Consumer productReported February 27, 2026 · The recalled children’s fingerpainting kits contain the hazardous substances methanol and ethylene glycol and are intended for children under 12 years of age... - TheKiddoSpace Recalls Children's Handwriting Practice Kits Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban
Consumer productReported February 27, 2026 · The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by... - TheKiddoSpace Recalls Children's Story Books Due to Choking Hazard
Consumer productReported February 27, 2026 · The recalled book's felt parts can detach, posing a choking hazard. - Grtard Magnetic Stick Figure Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported February 27, 2026 · The magnetic stick figure toy sets violate the mandatory standard for toys because they contain loose magnets, posing an ingestion hazard to children. When... - Bicystar High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violates Mandatory Standard for High Chairs
Consumer productReported February 27, 2026 · The high chairs violate the mandatory standard for high chairs because they were sold without the required attached crotch restraint, posing a deadly fall... - Magnetic Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Kaiwenshangpin
Consumer productReported February 27, 2026 · The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - Trankerloop Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violates Mandatory Standard for Infant Bath Seats
Consumer productReported February 27, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious... - Magnetic Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Yiruikeji2024
Consumer productReported February 27, 2026 · The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - Surreal Brands Recalls Children's Tubby Tots Fizzy Flask Bath Magic Bath Foam Sets Due to Impact Hazard
Consumer productReported February 27, 2026 · Moisture trapped inside the bath foam set container can cause pressure to build up, allowing pieces to be forcefully ejected when opened, posing an impact... - Somgem Pig and Yomin Toilet Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters; Sold on Amazon by Elepdv
Consumer productReported February 27, 2026 · The recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms... - Royal Oak Enterprises Recalls Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters
Consumer productReported February 27, 2026 · The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk... - Dupray USA Recalls Neat Steam Cleaners Due to Risk of Burn Hazards or Serious Injury
Consumer productReported February 27, 2026 · The steam cleaner's boiler can rupture if it is overfilled, corroded and the pressure release valve malfunctions, posing risk of burn hazards or serious injury... - PQL Recalls High Bay Linear LED Light Fixtures Due to Fire Hazard
Consumer productReported February 27, 2026 · The retaining pins used to secure the LED board inside some units can degrade, the LED board to come loose inside the fixture, posing a fire hazard. - Sanven Technology Recalls Vevor Baby Gates Due to Risk of Serious Injury from Entrapment Hazard; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported February 27, 2026 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset recall (Pure Solutions, Inc.)
FoodClass IIReported February 25, 2026 · Label declares bovine colostrum but does not declare milk allergen. - MOLLI 2 System System includes: MM1000 recall (Stryker Corporation)
Medical deviceClass IIReported February 25, 2026 · Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target... - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth... recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported February 25, 2026 · Due to damage to outer tray that can potentially compromise the sterile barrier - Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the... recall (Art Monkey LLC dba Why Not Natural)
FoodClass IReported February 25, 2026 · Potential to be contaminated with Salmonella - Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported February 25, 2026 · Products were mislabeled as the 6mm product but included the 5 mm product. - Medline Surgical Packs: 1) PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Gowns: 1) GOWN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Surgical Drapes: 1) SHEET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ARTHROSCOPY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SPINAL CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT UROLOGY SLING recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ROBOTIC GYN CDS-1 recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OB KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST/BREAST-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT ACES INSERT PEG recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) TOTE ABRAMS KNEE ARTHROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DENTAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OR ARTERIOGRAM recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ENDO KIT W/SYRINGE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SCC RF PAIN MGMT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANCILLARY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Estrone RIA recall (Immunotech A.S.)
Medical deviceClass IIReported February 25, 2026 · The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very... - Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and... - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - SAMIT Youth Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by SAMIT Outdoor
Consumer productReported February 19, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and... - Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging
Consumer productReported February 19, 2026 · The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium... - Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
Consumer productReported February 19, 2026 · The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children. - JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported February 19, 2026 · The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries... - Joly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
Consumer productReported February 19, 2026 · The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance... - Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
Consumer productReported February 19, 2026 · The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years... - Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Consumer productReported February 19, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Sodexo Stars Saccharin recall (Domino Foods Inc)
FoodClass IIIReported February 18, 2026 · Undeclared Aspartame - Sonic Tots recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Ore-Ida Tater Tots shaped potatoes recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. recall (Costco Wholesale Corporation)
FoodClass IReported February 18, 2026 · Undeclared hazelnut. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - UDENYCA recall (McKesson)
DrugClass IReported February 18, 2026 · Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the... - Cetrorelix Acetate for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIReported February 18, 2026 · Defective Delivery System: Missing or duplicated needles within the injection kit - Oxycodone Hydrochloride Tablets recall (Amerisource Health Services LLC)
DrugClass IIReported February 18, 2026 · Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities. - vancomycin HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - vancomycin HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - thiamine HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - ketamine HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - acyclovir sodium recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - Testosterone 100mg Anastrozole 4mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 87.5mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 200mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 100mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 75mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter