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. 1,184 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,184 in last 12 months

Showing 1801–1820 of 55,602 recalls

Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number:...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Recalled by Integra...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle Radiation Therapy Planning System: Multimodality Simulation...

The Issue: Due to a software issue, there is a potential image error of the Region of...

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
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· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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
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
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
FoodAugust 4, 2025· Neuhaus nv

Recalled Item: NEUHAUS brand ORIGINAL BELGIAN CHOCOLATE Recalled by Neuhaus nv Due to...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2025· B BRAUN MEDICAL INC

Recalled Item: Lactated Ringer's Injection USP Recalled by B BRAUN MEDICAL INC Due to Lack...

The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: Epinephrine Injection Recalled by PFIZER INC Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
FoodAugust 1, 2025· DFA Dairy Brands, LLC

Recalled Item: Carton Label: "Friendly's Vanilla Bean" Recalled by DFA Dairy Brands, LLC...

The Issue: Product contains undeclared wheat and soy.

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

Class II — Potential Health HazardOngoing
Refund