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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.
Showing 37521–37540 of 47,654 recalls
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...
The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...
The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Stability Specifications: Out of specification for preservative,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...
The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheryl's Buttercream Frosted Cut-Out BUNNY HEAD COOKIES Recalled by Cheryls...
The Issue: The cookie was packed in the incorrect film. The film that it was packed in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...
The Issue: During an internal inspection of the production process the firm discovered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...
The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.