Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,863 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,863 in last 12 months

Showing 82018220 of 55,602 recalls

DrugOctober 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...

The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...

The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...

The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2023· Safecor Health, LLC

Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%) Recalled by...

The Issue: CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 19, 2023· Tiffany Food Corp.

Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...

The Issue: Products are a choking hazard

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 19, 2023· Tiffany Food Corp.

Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...

The Issue: Products are a choking hazard

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 19, 2023· Tiffany Food Corp.

Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...

The Issue: Products are a choking hazard

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Pumpkin Spice Waffles Recalled by Nature'S Path Foods...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 19, 2023· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Dark Chocolate Chip Waffles Recalled by Nature'S Path...

The Issue: undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Abbott CELL-DYN Ruby Recalled by Abbott Laboratories Due to The devices...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...

The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· CardioQuip, LLC

Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...

The Issue: There is a potential for the heating-chamber to malfunction resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing