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. 934 recalls have been distributed to District of Columbia in the last 12 months.
Showing 37581–37600 of 47,654 recalls
Recalled Item: AMLODIPINE BESYLATE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to...
The Issue: Failed tablet specifications: One lot was found to contain oversized tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...
The Issue: The firm is recalling sterile enteral feeding syringes due to determining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic...
The Issue: Incorrectly packaged. Outer and inner labeling may incorrectly identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...
The Issue: A false negative result affecting the diagnosis may occur. A defect in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...
The Issue: Potential for weld disassociation of the cross pin, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...
The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...
The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...
The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange TAUT Intraducer Peritoneal Catheter 2mm x 1.6mm x...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange 10x40 Airway Stent System Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange FIBERWIRE SUTURE SCISSOR Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange Surgical Gown - Flyte Hood Pouch Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - 5.5mm BioComposite Corkscrew FT Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange 12MM VASCULAR Recalled by EXP Pharmaceutical...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange 3.5mm Threaded Cerclage Pin Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.