Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,357 recalls have been distributed to Wyoming in the last 12 months.
Showing 33461–33480 of 48,219 recalls
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.
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: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Presence of Particulate Matter: identified as cardboard.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: identified as a cloth fiber.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.