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 42761–42780 of 47,654 recalls
Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...
The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J.R. Jack Rabbit All Natural Herbal Supplement Recalled by Jack Rabbit, Inc...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY Recalled by...
The Issue: Terri Lynn Inc. "Deluxe Mixed Nuts No Peanuts" was found to have undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mixed nuts in a plastic bag labeled in part: Deluxe Mixed Nuts with...
The Issue: Terri Lynn Inc. "Deluxe Mixed Nuts No Peanuts" was found to have undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DeRoyal (R) Surgical Eye Spears Recalled by DeRoyal Industries Inc Due to...
The Issue: One lot of eye spears was labeled as being x-ray detectable, but contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...
The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it...
The Issue: Siemens determined that if an autosampler rack jam error occurs during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular...
The Issue: Due to a labeling error related to the conversion of the inner diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon 14 Microbore Extension Set with Bionector Recalled by Churchill...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Dressing Change Kit Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T8 REMOVAL HEAD Recalled by Medtronic Sofamor Danek USA Inc Due to One lot...
The Issue: One lot of the T8 Removal Head had incorrect hardness specification, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steinmann Pin Recalled by MicroAire Surgical Instruments, LLC Due to A...
The Issue: A medical device used in surgical procedures was packaged in a pouch in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kirschner-Wire (K-Wire) Recalled by MicroAire Surgical Instruments, LLC Due...
The Issue: A medical device used in surgical procedures was packaged in a pouch in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CALCIUM GLUCONATE 2 gm (PF) PRESERVATIVE FREE in 100 mL Recalled by...
The Issue: Non Sterility: Microbial contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All products Recalled by Specialty Compounding, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dove Chocolate Discoveries Fruit Collection Dark Chocolate - Covered...
The Issue: Cinnamon Dusted Dark Chocolate Almonds (Item Number: 3059D) were packaged in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VARISOURCE Breast Template System for high-dose rate Brachytherapy....
The Issue: The recall was initiated after Varian Medical became aware the Lexan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model BP7507 OPTI LION E-Plus Cassettes 25 Cassettes with Sample Probes...
The Issue: OPTI LION E-Plus Cassettes were labeled with an incorrect barcode. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonogage EyeScan Recalled by Sonogage Inc Due to During an FDA inspection on...
The Issue: During an FDA inspection on 7/15-26/2013, it was discovered that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exforge HCT (amlodipine Recalled by Novartis Pharmaceuticals Corp. Due to...
The Issue: Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.