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. 2,414 recalls have been distributed to Oklahoma in the last 12 months.
Showing 41801–41820 of 49,976 recalls
Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Unitized Catheter and Accessories...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z-HD (barium sulfate) For Suspension (98% w/w) Recalled by Bracco...
The Issue: Subpotent Drug: Low out of specification results for both pH and assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ibuprofen Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxcarbazepine Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HyVee applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile S.A....
The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...
The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Market Pantry Apple Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...
The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...
The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Market Pantry Apple Cinnamon Recalled by PUREFRUIT CHILE S.A Due to...
The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vanguard 360 Femoral Boss Reamer Recalled by Biomet, Inc. Due to The...
The Issue: The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.