Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,559 recalls have been distributed to Massachusetts in the last 12 months.
Showing 21961–21980 of 29,284 recalls
Recalled Item: Healing Abutment Dental implants Recalled by Biomet 3i, LLC Due to Pouches...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard Abutment Transfer Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
Recalled Item: Conical EP Twist Lock TM Coping Dental implants Recalled by Biomet 3i, LLC...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Micromini Flat Implant Cover Screw Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Preformance 15 degrees Pre-Angled Post Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: The ZYTO Tower is the input device to program the 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.
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.
Recalled Item: 30 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.