Recalls in Idaho (page 36)
3874 recalls.
- parodontax recall (Haleon US Holdings LLC)
DrugClass IIIReported February 4, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles. - Sterile Water for Irrigation recall (Baxter Healthcare Corporation)
DrugClass IIReported February 4, 2026 · Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution - BEAR Implant. Model Number: 1000. recall (Miach Orthopaedics)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be... - Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23 recall (LimFlow, Inc.)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date - SmartPath to dStream for XR and 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - SmartPath to dStream for 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Upgrade to MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T CX. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 1.5T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 1.5T. Product Codes recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Chest Drainage Units and Accessories: Product Code Description 1.... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported February 4, 2026 · The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.... - Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2 recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Conductivity Standard Solution Catalog/Model Numbers: 10001 recall (NIPRO Technical Services, Inc.)
Medical deviceClass IIReported February 4, 2026 · due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values... - PREGNANCY TEST 24CT recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Toothbrushes recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Feminine hygiene products recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Condoms recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Bandages and first aid kits: FIRST AID KIT 24/42PC recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Alphenix INFX-8000V recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000H recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000F recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000C recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - AlternatiV+ Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - AlternatiV+ Max Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Push-In Suture Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Dual Thread Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Fixone Biocomposite Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Fixone Hybrid Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Gazelle USA Recalls Urban Arrow FamilyNext Pro Cargo E-Bikes Due to Injury Hazard
Consumer productReported January 29, 2026 · The buckle can fail to fully latch when used with children in the cargo area, posing injury hazards to children. - Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements
Consumer productReported January 29, 2026 · The glue contains methanol, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The glue's packaging is not... - Viofairy Hair Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by FDA
Consumer productReported January 29, 2026 · The serum bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum's packaging is... - Primark Recalls The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets Due to Ingestion Hazard
Consumer productReported January 29, 2026 · The crayons in the coloring set have high levels of strontium and aluminum, and this may present a risk if ingested, posing a poisoning hazard if ingested by... - Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Drowning Hazard; Manufactured by Starmatrix Group Drowning Hazard; Manufactured by Starmatrix Group
Consumer productReported January 29, 2026 · The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk. - Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Choking Hazard
Consumer productReported January 29, 2026 · The legs of the plush toy can detach from the body allowing the release of small beads that are on the legs, posing a choking hazard to young children. - Northern Tool + Equipment Recalls Hot Water Pressure Washers Due to Fire Hazard
Consumer productReported January 29, 2026 · The fan wheel on the recalled pressure washers can fail, causing abnormal burner operation that can produce smoke and/or bursts of flames during use, posing a... - LuxJet Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Consumer productReported January 29, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin... - Mindbodygreen Recalls Ultimate Multivitamin+ Dietary Supplement Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported January 29, 2026 · The bottles are filled with dietary supplements containing iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging... - Rear Bolts on Trek and Electra Electric Bicycles Recalled Due to Fall Hazard; Manufactured by Hyena
Consumer productReported January 29, 2026 · The rear wheel bolts can break when torqued, causing the wheel to separate from the bicycle, posing a fall hazard. - AiTuiTui Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Vanfun
Consumer productReported January 29, 2026 · The hair growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum bottle is... - Sefudun 5% Minoxidil Hair Growth Serum Kits Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Nengmiaokeji
Consumer productReported January 29, 2026 · The hair growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The serum bottle is... - The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique... recall (Beckman Coulter Ireland, Inc.)
Medical deviceClass IIReported January 28, 2026 · Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent... - Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog... recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Due to probe bags that may have a compromised or incomplete sterile pouch seal. - Allwell Angioplasty Pack REF: IS-30-B1/B recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Merit Medical recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Merit Medical recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Merit Medical recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Merit Medical recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Allwell Inflation Device recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers:... recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure. - Icosapent Ethyl capsules recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported January 28, 2026 · Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules - Thyroid recall (Specialty Process Labs LLC)
DrugClass IIReported January 28, 2026 · Subpotent Drug - Furosemide Tablets recall (Graviti Pharmaceuticals Private Limited)
DrugClass IIReported January 28, 2026 · Presence of Foreign Substance - Diclofenac Sodium Topical Gel recall (Cipla USA, Inc.)
DrugClass IIIReported January 28, 2026 · Failed PH Specifications - Patient Information Center iX recall (Philips North America)
Medical deviceClass IIReported January 28, 2026 · A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - TS-10/TS-10H Tube Sorter recall (Sysmex America, Inc.)
Medical deviceClass IIReported January 28, 2026 · Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift. - Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius... recall (Tyber Medical)
Medical deviceClass IIReported January 28, 2026 · The supplier manufactured anatomical left plates with an incorrect thread orientation. - Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius... recall (Tyber Medical)
Medical deviceClass IIReported January 28, 2026 · The supplier manufactured anatomical left plates with an incorrect thread orientation. - Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b ... recall (LEASEIR TECHNOLOGIES SLU)
Medical deviceClass IIReported January 28, 2026 · The console label for affected devices is missing the "DANGER" symbol. - Mazor X robotic guidance system REF: TPL0059 recall (Mazor Robotics Ltd)
Medical deviceClass IIReported January 28, 2026 · Software errors that can result in incorrect surgical instrument positioning during spinal surgery. - SIGMA Spectrum Infusion Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported January 28, 2026 · Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - ICU Medical Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - GE Healthcare Omni Legend recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 28, 2026 · There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking... - Tego Connector: REF: 011-D1000 recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal... - Mikario Trading Convertible Baby Gyms Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standard for Infant Support Cushions; Sold on TikTok Shop
Consumer productReported January 22, 2026 · The recalled baby gyms violate the mandatory safety standard for infant support cushions because the floor mats can obstruct an infant's breathing, posing a... - Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen
Consumer productReported January 22, 2026 · The recalled spray bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging is... - Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported January 22, 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...