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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26321–26340 of 49,976 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT540. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Riomet (metformin hydrochloride oral solution) Recalled by Sun...
The Issue: Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MGBX ZESTAW GB LS X1 Product Usage: The Endo GIA Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX KITDE0183 APPENDIX LIPPE DETMOLD (KITDE0183) (2) KIT-DE-0083...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX LAPIMBGP1 ZESTAW DO MGBP (LAPIMBGP1) Product Usage: The Endo Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KIT00714 KIT SLEEVE Product Usage: The Endo GIA universal Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)LAPBARLECZNA ZESTAW BARIATRYCZNY LECZNA (2) KITBAR021- BARIATRIC KIT X1...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX 01KBAR006116V PROC BYPASS 01KBAR0061(Item Code 01KBAR006116V PROC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.