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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41881–41900 of 47,654 recalls
Recalled Item: Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB) Recalled by Arrow...
The Issue: Potential for a leak between the catheter and the bifurcate which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NH () API NH is a standardized system Recalled by Biomerieux France...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria () API Listeria is a standardized system Recalled by Biomerieux...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent () ZYM B reagent is an Recalled by Biomerieux France Chemin De...
The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Monitor Suspensions that may be on the following Fluoroscopic Recalled...
The Issue: Missing screws in the overhead Video Monitor Suspension. GE discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill...
The Issue: Following a retrospective review for Baxter Daytona Complaint CR-954, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 780 Hematology Analyzer Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the LH 750 and LH 780 Hematology Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaSafe Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the VersaSafe Extension Intravascular Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adipotrim XT Recalled by Deseo Rebajar Due to Undeclared Api
The Issue: Marketed Without an Approved NDA/ANDA: FDA lab results found undeclared API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carisoprodol Tablets Recalled by West-Ward Pharmaceutical Corp. Due to...
The Issue: Presence of Foreign Substance; heavy metals (chromium, titanium etc) and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Digestive enzyme capsules sold under the NOW Foods Recalled by NOW Foods Due...
The Issue: Digestive enzyme capsules manufactured by NOW Foods may contain the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ortho Molecular Products DigestzymeV. Dietary Supplement. Gastrointestinal...
The Issue: Ortho Molecular Products' vegetable enzyme vendor issued a recall of the raw...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...
The Issue: There exists a software issue associated with patient selection from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...
The Issue: EOS imaging discovered during production internal testing that the X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...
The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: During routine stability testing one tablet was found with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sumatriptan Succinate Injection Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imitrex STATdose System Recalled by GlaxoSmithKline, LLC. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets USP 0.5 mg. Rx Only Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Moisture Limit; Out of Specification (OOS) results were obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.