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. 1,050 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16861–16880 of 49,976 recalls
Recalled Item: Covidien TA Auto Suture Vascular Loading Unit with DST Series Recalled by...
The Issue: May contain a damaged internal component which could impede staple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien TA Auto Suture Vascular Stapler with DST Series Technology Recalled...
The Issue: May contain a damaged internal component which could impede staple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: Failed Impurity/Degradation Specifications: Unidentified impurities not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 5 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 11 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...
The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Good & Gather Banana Chocolate Chip Date & Nut Bars Recalled by Riverside...
The Issue: The product contains an undeclared almonds.
Recommended Action: Do not consume. Return to store for a refund or discard.