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. 2,885 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,885 in last 12 months

Showing 50815100 of 55,602 recalls

DrugAugust 5, 2024· Zeco LLC

Recalled Item: HAND-I-SAN Recalled by Zeco LLC Due to CGMP Deviations: sterile water not...

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2024· QUANTUM SURGICAL SAS

Recalled Item: The EPIONE device v1.0.2 is a user controlled Recalled by QUANTUM SURGICAL...

The Issue: Quantum Surgical has become aware that a component (central axis) inside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· MICROVENTION INC.

Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...

The Issue: Due to Retrieval Device product labels stating the incorrect expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: ImpellaCP SmartAssistSetAPAC Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 SmartAssist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Pump 381 Pump Set (US) Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set APAC Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing