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. 2,660 recalls have been distributed to District of Columbia in the last 12 months.
Showing 421–440 of 47,654 recalls
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baraka French Style Puff Pastry 1lb and 1.5lbs sizes Recalled by ZIYAD...
The Issue: May contain partially hydrogenated oils
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baraka Gourmet Pastry Kunafe 6.7oz. Recalled by ZIYAD BROTHERS IMPORTING Due...
The Issue: May contain partially hydrogenated oils
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) Recalled by...
The Issue: Lack of Assurance of Sterlity
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Dual Thread Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.