Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,491 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,491 in last 12 months

Showing 2068120700 of 28,355 recalls

Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREC PRM 18FR 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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover CATCH KIT SOAP Item Code: 5205 Castile soap 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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing