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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,679 in last 12 months

Showing 2574125760 of 29,947 recalls

Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Handicare USA, Inc.

Recalled Item: ReTurn 7500/7500 Aid Recalled by Handicare USA, Inc. Due to During the...

The Issue: During the period of April 2009  May 2011, Handicare AB used a wing handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Arrow International Inc

Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...

The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Tenex Health Inc

Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...

The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...

The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Ivoclar Vivadent, Inc.

Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...

The Issue: A stock check revealed broken glass fibers between the connector and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to Recalled by...

The Issue: It was determined that under rare environmental conditions (i.e., extremely...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2014· Blue Belt Technologies MN

Recalled Item: NavioPFSTM System Recalled by Blue Belt Technologies MN Due to Blue Belt...

The Issue: Blue Belt Technologies is conducting a voluntary recall for their Navio PFS...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...

The Issue: Naturalyte Liquid Bicarbonate maybe contaminated

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...

The Issue: Software anomaly: potential for delay in the reporting of patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...

The Issue: Potential for biased results when a Multiple Window (MW) code is associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing