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. 997 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
997 in last 12 months

Showing 39741–39760 of 55,602 recalls

Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Gingihue 15 degrees Pre-Angled Post 4mm(D) x 5mm(P) x 2mm(H) Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: DAL-RO Housing Recalled by Biomet 3i, LLC Due to Pouches may not have been...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain EP Pick-Up Coping Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Straight Healing Abutment 4.1mm(D) x 4.1mm(P) x 4mm(H) Item:ISHA44...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Provide Protection Cap Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Conical 25 degree Angled Abutment Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Pick-up Coping Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Gingihue Post 4.1mm(D) x 5mm(P) x 4mm(H) Item: IAPP454G Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Conical 17 degree Angled Abutment Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Bellatek Encode Healing Abutment Dental implants Recalled by Biomet...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Straight Pick-Up Coping 5.0mm(D) x 0mm(P) Item:IWIP50 Dental...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Conical EP Healing Cap Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2015· Golden State Medical Supply Inc.

Recalled Item: MECLIZINE HYDROCHLORIDE TABLETS Recalled by Golden State Medical Supply Inc....

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2015· Golden State Medical Supply Inc.

Recalled Item: MECLIZINE HYDROCHLORIDE TABLETS Recalled by Golden State Medical Supply Inc....

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 24, 2015· Zimmer, Inc.

Recalled Item: Persona EM Distal Rod Recalled by Zimmer, Inc. Due to Complaints that the...

The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...

The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2015· Zimmer, Inc.

Recalled Item: Persona EM Proximal Tube Recalled by Zimmer, Inc. Due to Complaints that the...

The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· ZYTO Technologies, Inc.

Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...

The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Biomerieux Inc

Recalled Item: Granada Biphasic Broth The product is a selective medium for Recalled by...

The Issue: FDA has determined that the product requires 510(k) clearance to continue...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Intuitive Surgical, Inc.

Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...

The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...

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

Class II — Potential Health HazardOngoing