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. 2,919 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,919 in last 12 months

Showing 11011120 of 55,602 recalls

Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2025· Mohamed Hagar

Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 8, 2025· Tai Foong USA Inc

Recalled Item: Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 Recalled...

The Issue: Undeclared shrimp

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 8, 2025· Sprouts Farmers Market

Recalled Item: Sprouts Smoked Mozzarella Pasta Salad Recalled by Sprouts Farmers Market Due...

The Issue: Product may contain Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 8, 2025· ASTRAZENECA PHARMACEUTICALS

Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...

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 DeviceOctober 8, 2025· Cellavision AB

Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...

The Issue: Automated cell-locating device barcode reader may read the barcode of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...

The Issue: The device may either fail to start up, or the transducer may start briefly...

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

Class II — Potential Health HazardOngoing
FoodOctober 7, 2025· Eagle Spice and Extract Co., Inc.

Recalled Item: Eagle Spice Ground Ginger 16 oz. Recalled by Eagle Spice and Extract Co.,...

The Issue: Contains elevated levels of lead (Pb)

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Rising Pharma Holding, Inc.

Recalled Item: Carbidopa Recalled by Rising Pharma Holding, Inc. Due to Product mix up:...

The Issue: Product mix up: complaint received that sealed medication bottle contained...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2025· Philips Respironics, Inc.

Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...

The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· NeuroLogica Corporation

Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...

The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...

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

Class II — Potential Health HazardOngoing