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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 14481–14500 of 49,976 recalls
Recalled Item: VIDAS Clostridium Difficile GDH Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS DEX@ Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 is multi-functional general R/F systems. Recalled by...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Lyme IgM II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...
The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Surgical systems with the following Model Name/ Recalled by...
The Issue: Issue was identified during internal engineering evaluation. Use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 is multi-functional general R/F systems. Recalled by...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Clostridium Difficile Toxin A&B Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Measles IgG (MSG) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...
The Issue: Incorrect expiration date on its package labeling (shipper box and inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.