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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45481–45500 of 47,654 recalls
Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...
The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...
The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to It has...
The Issue: It has been determined that, in some cases, pulley drive components have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic...
The Issue: The items in this lot are missing the ion implantation feature. The surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 13.0 thru 20.0 Recalled by Biomet, Inc....
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Operations,...
The Issue: On cobas c 701 and cobas c 702 modules of the Cobas 8000 series analyzer, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 8.0 THRU 12.5 Recalled by Biomet, Inc....
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Non-Sterile Products manufactured by Ameridose LLC Recalled by Ameridose...
The Issue: GMP deficiencies
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Sterile Products manufactured by Ameridose LLC Recalled by Ameridose LLC...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WP Saki Ika Cuttlefish JFC# 15603 Recalled by J F C International Inc Due to...
The Issue: JFC International is recalling WelPac Saki Ika Cuttlefish because of mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WP Saki Ika Cuttlefish Hot JFC# 15606 Recalled by J F C International Inc...
The Issue: JFC International is recalling WelPac Saki Ika Cuttlefish because of mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: This notice is being provided in follow up to the field correction initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posey Biothane Restraint Cuffs Recalled by J T Posey Company Due to The firm...
The Issue: The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...
The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical RUMI Arch Recalled by Cooper Surgical, Inc. Due to Excessive...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Advincula Arch Recalled by Cooper Surgical, Inc. Due to...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous Fixation System (IFS) 1.7 mm Recalled by Orthohelix Surgical...
The Issue: The firm was notified by a customer that there was a burr on the inside end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Stationary radiographic system Recalled by Philips...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system...
The Issue: With Digital Diagnost R2.0.2 a mirrored "R in a circle" is burnt into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Alara Pharmaceutical Co Due to...
The Issue: Subpotent; 15 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.