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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42441–42460 of 47,654 recalls
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Oxidized stainless steel found in vial of 1%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Hospira, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Confirmed customer report of leakage of vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets Recalled by...
The Issue: Failed Dissolution Specification:12 hour time point at 18 months of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...
The Issue: PENTAX Medical has become aware of a product issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR ActiveTrak Excimer Laser System Recalled by Abbott Medical Optics, Inc....
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: Recalled by...
The Issue: Sekisuki Diagnostics has issued a Product Correction for certain lot numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 3g/60 mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 1g/20mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.