Product Recalls in Washington
Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,939 recalls have been distributed to Washington in the last 12 months.
Showing 21961–21980 of 29,208 recalls
Recalled Item: Certain EP Healing Abutment Dental implants Recalled by Biomet 3i, LLC Due...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Non-Hexed Implant Pick-up Coping 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: IOL Titanium Temporary Cylinder 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: O-Ring Abutment 4.1mm(D) x 4mm(H) Item: OSO40 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: Locator Extended Range Males 4pk 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: O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 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 Abutment Pick-up 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: Standard 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: Certain Gingihue 15 degree Angled Post 4.1mm(D) x 5mm(P) x 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: Cover Screw 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: LDA Screw SBL 4mm(D) Item: SCRSBL2 Dental implants Recalled by Biomet 3i,...
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: 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.
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: 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: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...
The Issue: "The public reason for the recall is that the product is being recalled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.