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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 39881–39900 of 47,654 recalls
Recalled Item: American Spoon Food Sour Cherry Marmalade Recalled by American Spoon Foods,...
The Issue: Product may have mold in jar.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...
The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...
The Issue: The bed head deck may fail to elevate as expected during normal operation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....
The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133 Recalled by Unique...
The Issue: Non-Sterility: One lot of N-Acetyl Cysteine vials tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All sterile products within expiry Recalled by Unique Pharmaceutical, Ltd...
The Issue: Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine HCl Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Label Error On Declared Strength: The side label description...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a...
The Issue: This remedial action is the result of six product complaints associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...
The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs...
The Issue: Customers may receive positively biased results when using VITROS¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some sheets...
The Issue: Some sheets of the medical screen film are fogged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...
The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for the blue endo MOREsolution Electromechanical...
The Issue: Some pages of the Instructions for Use were omitted, including pages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.