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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 31141–31160 of 47,654 recalls
Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...
The Issue: The firm sent the Technical Bulletin to consignees who received the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection Recalled by Hospira Inc., A...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection Recalled by Hospira Inc., A Pfizer...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PREMARIN (conjugated estrogen tablets Recalled by Pfizer Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...
The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: Image data for a patients image may not be correct
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...
The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...
The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released...
The Issue: Roche Diabetes Care, Inc. initiated a voluntary recall for the version 1.2.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...
The Issue: Customers complained of low/empty reagent vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: potential failure to meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed...
The Issue: Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate
Recommended Action: Do not consume. Return to store for a refund or discard.