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. 2,488 recalls have been distributed to Iowa in the last 12 months.
Showing 20461–20480 of 28,127 recalls
Recalled Item: Covidien Dover PREM U/M 14FR TMP SNS CSD Item Code: Recalled by Covidien LLC...
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 PRECISION PRM 18FR SIL COUDE CATH SECURE Item Recalled by...
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 PREC PRM 16FR SILVER FLY TY Item Code: Recalled by Covidien...
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 7 OZ MIDSTREAM W/CAST SOAP Item Code: 24035 Recalled by...
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 P400 PREM U/M 16FR SIL COUDE CATH SECURE Recalled by Covidien...
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: 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: Endobon-Xenograft Granules Recalled by Biomet France SARL Due to...
The Issue: Cytotoxicity tests were not passed at 36 months. Use of Endobon-Xenograft...
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.