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 2422124240 of 29,947 recalls

Medical DeviceDecember 4, 2014· Zimmer Manufacturing B.V.

Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...

The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Zimmer, Inc.

Recalled Item: Persona Cemented Tibial Broach Inserter/Extractor. The Persona Cemented...

The Issue: The affected lot was supplied by contract manufacturer and are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...

The Issue: Suboptimal routing of the cable may result in increased wear over time....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Artifacts are found in acquired imaging on the SOMATOM Force.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Medtronic Sofamor Danek USA Inc

Recalled Item: POWEREASE Instruments Set Screw Breakoff Instrument Recalled by Medtronic...

The Issue: The retaining tabs component of the Set Screw Retaining Drive may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUX Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUX Material Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing