Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,800 recalls have been distributed to Iowa in the last 12 months.
Showing 34761–34780 of 49,990 recalls
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...
The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...
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: 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: 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: 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 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 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: 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: 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: 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: 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 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: 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 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: 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: 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: 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: 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.