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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.
Showing 1341–1360 of 47,654 recalls
Recalled Item: Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300....
The Issue: Potential for compromised integrity of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...
The Issue: Firm has identified a security vulnerability in AW Server products. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL) Recalled by Sandoz Inc...
The Issue: cGMP deviations: Temperature excursion during transportation.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....
The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in...
The Issue: Product may contain undeclared shrimp (crustacean shellfish).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item number/ Product description AKGN82E GENERAL...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...
The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medical convenience kits UDPG88W PICC G-TUBE PACK-230209 Recalled by...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.