Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,827 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,827 in last 12 months

Showing 3650136520 of 52,570 recalls

DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...

The Issue: Presence of Particulate Matter: identified as dried skin.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
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