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. 2,485 recalls have been distributed to Oklahoma in the last 12 months.
Showing 24801–24820 of 49,976 recalls
Recalled Item: Finafta Baby Recalled by Product Quest Manufacturing LLC Due to CGMP...
The Issue: CGMP Deviations: products manufactured under conditions that could impact...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TopCare Recalled by Product Quest Manufacturing LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: products manufactured under conditions that could impact...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications - OOS was observed for ATV...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ipamorelin 3 mg Lyophilized 1 vial 1109 East Hallandale Beach Recalled by...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin 10 mg vial Lyophilized 1109 East Hallandale Beach Blvd....
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 6000 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ipamorelin 9 mg vial Lyophilized 1109 East Hallandale Beach Blvd. Recalled...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...
The Issue: 3D projections may be incorrect when the pair of images used is a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.