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 2454124560 of 29,947 recalls

Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· GE Inspection Technologies, LP

Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...

The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· CSA Medical

Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...

The Issue: An increase in complaint trending for a loss of audible sound associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Ion Beam Applications S.A.

Recalled Item: adaPT insight (12C) Recalled by Ion Beam Applications S.A. Due to Two issues...

The Issue: Two issues were identified: 1. In the release of adaPT insight v1.3.2., the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Breas Medical AB

Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...

The Issue: Unintended treatment termination could result from a keypad malfunction in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...

The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Infusion Set Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: AC TenderLink 13/30 10 pcs Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Contact Detach Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Silhouette Paradigm 13mm Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Comfort 5+5 Pack w/110cm Tube & 17mm Cann. UPC# 3-89110-14147-7 Recalled by...

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: SureT G29 6mm Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Synthes (USA) Products LLC

Recalled Item: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...

The Issue: The device may operate solely in reverse mode, not operate in reverse mode...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· Abbott Medical Optics Inc (AMO)

Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...

The Issue: AMO has received complaints where the finger grip dislodged while depressing...

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

Class II — Potential Health HazardOngoing