Recalls in Iowa (page 16)
3929 recalls.
- Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported July 8, 2026 · cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI). - Dextroamphetamine Saccharate recall (Lannett Company Inc.)
DrugClass IIReported July 8, 2026 · Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. - Lidocaine HCl Injection USP recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Accucaine recall (Asclemed USA Inc.)
DrugClass IIReported July 8, 2026 · Lack of Assurance of Sterility - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported July 8, 2026 · Subpotent Drug - prednisoLONE Acetate Ophthalmic Suspension recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported July 8, 2026 · Presence of Foreign Substance - Fexofenadine Hydrochloride Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported July 8, 2026 · Failed Impurities/Degradation Specifications - IMULDOSA recall (ACCORD BIOPHARMA INC)
DrugClass IIReported July 8, 2026 · Lack of assurance of Sterility: - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - ChloraPrep FREPP recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Radius VSM Disposable NIBP Cuff recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Radius VSM ECG pre-connected Set recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Solar GI System recall (Laborie Medical Technologies Corp)
Medical deviceClass IIReported July 8, 2026 · Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's... - Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 recall (Carl Zeiss Meditec AG)
Medical deviceClass IIReported July 8, 2026 · Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. - RayCare 2024A SP4. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - RayCare 2024A SP1. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - ARTIS icono floor. Model Number: 11327700. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono biplane. Model Number: 11327600. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - Adapter for Head Positioning recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported July 8, 2026 · The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of... - CRE Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - IntelliCuff recall (Hamilton Medical AG)
Medical deviceClass IIReported July 8, 2026 · Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the... - Medtronic Harmony Delivery Catheter System recall (Medtronic Heart Valves Division)
Medical deviceClass IReported July 8, 2026 · Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system... - GC Agar Base recall (Remel, Inc)
Medical deviceClass IIReported July 8, 2026 · Reduced or no recovery of some strains of Neisseria gonorrhoeae. - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - Short Monobloc Stem Broaches recall (Medacta Usa Inc)
Medical deviceClass IIReported July 8, 2026 · Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the... - Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH recall (Medline Industries, LP)
Medical deviceClass IReported July 8, 2026 · Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on... - Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA -... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Omnipod recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.... recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA P.CIRCUIT 5KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL LINE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURING SET recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) IMAGING BIOPSY TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) STD recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) DYNJ0621189X recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MULTIMED recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) BLOCK TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Winco Fireworks International Recalls Roman Candles 8 Shot Fireworks Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 3, 2026 · The recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. - Winco Fireworks International Recalls Unity 7 Shot 200 Gram Aerial Cake Fireworks Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 3, 2026 · The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards. - Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
Consumer productReported July 3, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store
Consumer productReported July 3, 2026 · The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin... - Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fire Hazard
Consumer productReported July 3, 2026 · The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard. - Target Recalls Gigglescape™ Under the Sea Popping Toy Due to Choking Hazard
Consumer productReported July 3, 2026 · The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard. - AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions; Sold on Amazon by Pretty-Life
Consumer productReported July 3, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support... - Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported July 3, 2026 · The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards. - Projecting LED Finger Light Toys Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by POPOOO
Consumer productReported July 3, 2026 · The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by... - Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported July 3, 2026 · The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging... - Topyond Pool Drain Ports with Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold by Jialyduu
Consumer productReported July 3, 2026 · The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly... - Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for Infant Sleep Products
Consumer productReported July 3, 2026 · The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed... - 25# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/NS recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 8/9.5oz Tub Nut - Sunflower Seed recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.