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 51015120 of 55,602 recalls

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
DrugAugust 2, 2024· EMPOWER CLINIC SERVICES LLC

Recalled Item: Empower Pharmacy Recalled by EMPOWER CLINIC SERVICES LLC Due to Lack of...

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 DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Bard Peripheral Vascular Inc

Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...

The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2024· Baxter Healthcare Corporation

Recalled Item: Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection) Recalled by...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2024· Amneal Pharmaceuticals, LLC

Recalled Item: Methotrexate Tablets Recalled by Amneal Pharmaceuticals, LLC Due to Presence...

The Issue: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 1, 2024· Outset Medical, Inc.

Recalled Item: Tablo Console Recalled by Outset Medical, Inc. Due to Blood leak sensor, a...

The Issue: Blood leak sensor, a component of hemodialysis device, may show decreased...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV LL 18X103- Wallflex Esophageal Partially Recalled...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW PC 23MM X 6.2CM IN 18.5 FR- Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 23/28MM X 105MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX12CM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX15CM- Agile Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV LL 23X155- Wallflex Esophageal Partially Recalled...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix M50 instrument -Intended for the rapid identification (ID)...

The Issue: Escherichia coli (E. coli) misidentification for clinical samples that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX15CM-Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 18/23MM X 123MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV 18X103MM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV 23X155MM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO FC RMV 23MM X 6.2CM IN 18.5 FR-Agile Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing