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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16821–16840 of 28,654 recalls
Recalled Item: Dimension¿ Sirolimus (SIRO) Flex¿ reagent cartridge Recalled by Siemens...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ HBc IgM Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to...
The Issue: Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO-KATH Epidural Catheter Set Recalled by Epimed International Due to...
The Issue: Potential for stylet to protrude from the distal end of the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO-KATH(TM) Caudal Set Recalled by Epimed International Due to Potential...
The Issue: Potential for stylet to protrude from the distal end of the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...
The Issue: Communication-connection error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...
The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...
The Issue: Reports of product loosening or coming unscrewed from the handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...
The Issue: During continuous postmarket surveillance activities, we have noticed a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...
The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System STER TROC LAG SCR 70 MM Recalled by Zimmer...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X Recalled by Zimmer...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD and and Xper FD ORT - Philips Recalled by Philips Electronics...
The Issue: Extra monitors, so called 7th or 8th monitor, mounted on the Monitor Ceiling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...
The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.