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. 2,906 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,906 in last 12 months

Showing 17811800 of 55,602 recalls

FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2025· Cepheid

Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...

The Issue: As a result of Post-Market half-time stability testing, false negative test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000....

The Issue: Reports of out-of-box failures discovered during the limited launch phase....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Olympus Corporation of the Americas

Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....

The Issue: Potential for undetected, deformed a-traumatic tips.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to...

The Issue: Inserter, used as part of a system with an intervertebral body fusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
FoodAugust 5, 2025· M.O.M Enterprises, LLC.

Recalled Item: Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Due to...

The Issue: Potential for spoilage due to yeast contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2025· Haleon US Holdings LLC

Recalled Item: Sensodyne PRONAMEL (Potassium nitrate 5% Recalled by Haleon US Holdings LLC...

The Issue: Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is...

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Spironolactone Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Presence of foreign substance: identified as aluminum.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.

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

Class II — Potential Health HazardOngoing