Product Recalls in New Hampshire
Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,409 recalls have been distributed to New Hampshire in the last 12 months.
Showing 20341–20360 of 27,899 recalls
Recalled Item: Covidien Dover P400 PREM U/M 18FR SIL FLY 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 PREC PRM 14FR 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 MIDSTREAM KIT CASTILE SOAP Item Code: 2090SA Castile Recalled...
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: 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.
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.