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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.
Showing 681–700 of 47,654 recalls
Recalled Item: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varenicline Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Sub...
The Issue: Sub potent drug: during the 9-month stability test conducted, the assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard ORGAN RECOVERY OR PACK Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard MINI PLUS KIT SOUTH Recalled by AVID Medical, Inc. Due to Devices...
The Issue: Devices are not suitable for organ transplant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXLOCK Achilles Repair Implant Kits Recalled by Medline Industries, LP Due...
The Issue: There have been multiple complaints of drill bit fusing to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...
The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams Recalled by...
The Issue: Contaminated with Clostridium botulinum
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad...
The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Costco Item# 19927 Kirkland Signature Caesar Salad Recalled by Costco...
The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carton label: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA, Inc...
The Issue: Defective Container - A defect in the side-seal which allows leakage of product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...
The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...
The Issue: Due to a number of modules flashed with a date and time associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...
The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...
The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.