Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34381–34400 of 47,654 recalls
Recalled Item: IOL Abutment and Screw 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: Drill Stop Dental implants Recalled by Biomet 3i, LLC Due to Pouches may not...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain EP Healing Abutment 5mm(D) x 5.6mm(P) x 4mm(H) Item: 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: Provide Impression 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.
Recalled Item: O-Ring Abutment 4.1mm(D) x 6mm(H) Item: OSO60 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: Gold-Tite Square Uniscrew Item: UNISG 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: 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.
Recalled Item: Standard 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: Implant 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 Pick-Up Coping 4.1mm(D) x 5mm(P) Item: IIIC12 Dental implants...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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: 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: 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 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.