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 1421–1440 of 55,602 recalls

Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: TENACIO Pump with InhibiZone Recalled by Boston Scientific Corporation Due...

The Issue: The potential for devices to experience inflation and/or deflation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Insulet Corporation

Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...

The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

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

Class II — Potential Health HazardOngoing
FoodSeptember 10, 2025· Gooder Foods, Inc.

Recalled Item: GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET...

The Issue: Undeclared allergens (milk).

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 10, 2025· Gooder Foods, Inc.

Recalled Item: GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS...

The Issue: Undeclared allergens (cashews).

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2025· Medline Industries, LP

Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...

The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· Biomet, Inc.

Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...

The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· MedicalCommunications GmbH

Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...

The Issue: Potential that the measured value may be smaller than the actual area.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2025· Draeger, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...

The Issue: The device either indicated a failure of the piston ventilator before use or...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 9, 2025· Draeger, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...

The Issue: The device either indicated a failure of the piston ventilator before use or...

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

Class I — Serious Health HazardOngoing
FoodSeptember 9, 2025· WFM Purchasing, LP

Recalled Item: Whole Foods Market Blueberry Almond Granola Recalled by WFM Purchasing, LP...

The Issue: Product was incorrectly labeled, resulting in undeclared wheat, sesame, and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemosafeLock Vial Adapter : KL-VA001U3 KL-VA002U3 KL-VA131U3...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock" Port Recalled by ICU Medical, Inc. Due to Port weld...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemosafeLock Connecter Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· Beckman Coulter, Inc.

Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...

The Issue: Automated pipetting, diluting and specimen processing workstations for flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/2 ChemoLock" Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing