Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 28041–28060 of 28,654 recalls
Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 8 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 6 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 7 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 10 Packaging: The product was packaged within Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 1 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 27mm UPN Outer Box:...
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 4 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.