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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34081–34100 of 47,654 recalls
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...
The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...
The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUEL UP PLUS Recalled by Reesna, Inc Due to Undeclared Hydroxythiohomosildenafil
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUEL UP HIGH OCTANE Recalled by Reesna, Inc Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...
The Issue: FATwater bottles, Lemon flavor, are recalled due to microbial growth...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...
The Issue: FATwater bottles, Berry flavor, are recalled due to microbial growth...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FATwater bottle Recalled by Bulletproof Digital Inc Due to Potential E. coli...
The Issue: FATwater bottles, Tangerine flavor, are recalled due to microbial growth...
Recommended Action: Do not consume. Return to store for a refund or discard.