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. 1,737 recalls have been distributed to District of Columbia in the last 12 months.
Showing 33241–33260 of 47,654 recalls
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoledronic Acid Injection Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Lack of Assurance of Sterility; defective seals where the metal silver ring...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...
The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosupps Dr. Jekyll INTENSE PUMP PRE WORKOUT Recalled by ProSupps USA LLC...
The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: L'Bri Pure N' Natural Nutri Aloe Health Juice Drink 960 Recalled by Cosmetic...
The Issue: Product contains ingredients that are not on the label including sodium...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosupps Dr. Jekyll Recalled by ProSupps USA LLC Due to Mislabeling
The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 30 SERVINGS WATERMELON Recalled...
The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS ORANGE Recalled by...
The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS BLUERAZZ Recalled...
The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...
The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...
The Issue: Alcon is conducting a voluntary medical device correction of all VERION...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Sagent Pharmaceuticals Inc Due to Cross...
The Issue: Cross contamination with other products: metronidazole
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: col-rite (docusate sodium) stool softener softgels Recalled by Allegiant...
The Issue: Superpotent Drug: High out of specification results for assay at the 6 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...
The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...
The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...
The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.