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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.
Showing 3181–3200 of 28,654 recalls
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cysto Recalled by American Contract Systems, Inc. Due to ACS identified that...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bilateral Tubal Ligation Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal Delivery Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR Procedure Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.7 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACEMAKER PACK Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shoulder Recalled by American Contract Systems, Inc. Due to ACS identified...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.