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. 2,691 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,691 in last 12 months

Showing 2428124300 of 29,947 recalls

Medical DeviceNovember 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...

The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Zimmer Manufacturing B.V.

Recalled Item: Bone Screw Recalled by Zimmer Manufacturing B.V. Due to Analysis of returned...

The Issue: Analysis of returned complaint devices, product in inventory, and device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Becton Dickinson & Co.

Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...

The Issue: The products may exhibit indications of excessive oxidation. Excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Phadia US Inc

Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...

The Issue: During an investigation of instrument logs it was determined that In...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Cyberonics, Inc

Recalled Item: Cyberonics VNS Therapy AspireHC Recalled by Cyberonics, Inc Due to The...

The Issue: The recalled product was distributed with an incorrect serial number printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Philips Medical Systems, Inc.

Recalled Item: Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by...

The Issue: VCG battery ignited in a VCG unit when recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...

The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...

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

Class II — Potential Health HazardOngoing