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. 2,878 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,878 in last 12 months

Showing 54815500 of 55,602 recalls

Medical DeviceJuly 4, 2024· ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL

Recalled Item: FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM...

The Issue: During the assembly of the FRT250 cartridge assembly, an incorrect component...

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2024· Costco Wholesale Corporation

Recalled Item: The recalled product is mis-labeled as Ancient Grain + Vegetable Recalled by...

The Issue: Undeclared Almond and Soy. The Grain + Celery Salad with Apple Cider...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 3, 2024· TAILSTORM HEALTH INC

Recalled Item: Lidocaine HCL Injection Recalled by TAILSTORM HEALTH INC Due to Subpotent...

The Issue: Subpotent Drug: reduced efficacy for epinephrine

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2 Recalled by...

The Issue: It was confirmed that fibrinogen in patient plasma samples precipitates out...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...

The Issue: If the Sensis documentation functionality is used during adding of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2024· W.L. Gore & Associates, Inc.

Recalled Item: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for...

The Issue: Devices were labeled with an expiration date of four years and ten days...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...

The Issue: If the Sensis documentation functionality is used during adding of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...

The Issue: If the Sensis documentation functionality is used during adding of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Vibe systems with software version VD15B-Intended to be used Recalled...

The Issue: If the Sensis documentation functionality is used during adding of...

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

Class II — Potential Health HazardOngoing
FoodJuly 2, 2024· Sheetz Inc dba Sheetz Brothers Kitchen

Recalled Item: Shweetz Bakery-To-Go brand Peanut Butter Brownie Cheezecake Mashup Cookie...

The Issue: Undeclared peanuts

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Novel Laboratories, Inc. d.b.a Lupin Somerset

Recalled Item: PEG-3350 Recalled by Novel Laboratories, Inc. d.b.a Lupin Somerset Due to...

The Issue: Defective container: potential for non-sealed pouches which can lead to...

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...

The Issue: Cross contamination with other products.

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...

The Issue: Cross contamination with other products.

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Cross contamination with other products

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Cross contamination with other products

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Decitabine for Injection 50mg per vial Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Out of Specification for Total Aerobic Microbial Count...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2024· Argon Medical Devices, Inc

Recalled Item: BioPince Ultra Full Core Biopsy Instrument: : 360-1080-01 Recalled by Argon...

The Issue: Holes have been identified in biopsy instrument packaging trays compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2024· Stryker Sustainability Solutions

Recalled Item: Disposable 5 Lead Cable and Lead Wire System Recalled by Stryker...

The Issue: Disposable 5 lead cable and lead wire system package that should contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: LUMINOS Lotus Max -Intended to visualize anatomical structures by converting...

The Issue: The support arm may unintentionally lower resulting in injury to persons...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max -Intended to visualize anatomical structures by converting...

The Issue: The support arm may unintentionally lower resulting in injury to persons...

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

Class II — Potential Health HazardOngoing