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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.
Showing 33641–33660 of 47,654 recalls
Recalled Item: Covidien Dover MIDSTREAM KIT CASTILE SOAP Item Code: 2090SA Castile Recalled...
The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Dover MIDSTREAM KIT CASTILE SOAP Item Code: 2040SA Castile Recalled...
The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Recalled by Accuray Incorporated Due to The gun box...
The Issue: The gun box mounting bracket may fail to support the weight of the gun box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: identified as a cloth fiber.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Presence of Particulate Matter: identified as cardboard.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...
The Issue: Presence of Particulate Matter: identified as dried skin.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.