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 23212340 of 55,602 recalls

Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: a. Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 13, 2025· Volcano Corp

Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...

The Issue: Reports of IVUS catheter and guide wire entanglement during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Immunotech A.S.

Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...

The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...

The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...

The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...

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

Class II — Potential Health HazardOngoing
FoodJune 11, 2025· Vita Warehouse Corp.

Recalled Item: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Recalled by Vita...

The Issue: Contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 11, 2025· Macleods Pharmaceuticals Ltd

Recalled Item: Famciclovir Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Presence...

The Issue: Presence of Foreign Substance- Black hair strand found attached to a tablet...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit. Recalled by AVID...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: ROBOTIC PROSTATECTOMY PACK. Medical convenience kit. Recalled by AVID...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: HVI CARDIAC ROBOT PACK. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: GENERAL ROBOTIC PACK. Medical convenience kit. Recalled by AVID Medical,...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: GYN ROBOTIC PACK. Medical convenience kit. Recalled by AVID Medical, Inc....

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· AVID Medical, Inc.

Recalled Item: LAP CHOLE PACK. Medical convenience kit. Recalled by AVID Medical, Inc. Due...

The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,...

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

Class II — Potential Health HazardOngoing