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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16621–16640 of 49,976 recalls
Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...
The Issue: The instruments may become cold welded together when the drill is inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUR SPECIALTY Recalled by Rich Products Corp Due to Undeclared Wheat
The Issue: Product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 9" French Silk Base Recalled by American Blue Ribbon Holdings LLC Due to...
The Issue: Undeclared Pecan
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The EOSedge system may acquire two simultaneous orthogonal planar images...
The Issue: Inadequate images resizing and 2D measurement errors may occur when biplanar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used Recalled by...
The Issue: FUJIFILM has become aware that incorrect concentration values were printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection Recalled by...
The Issue: Lack of assurance of sterility: The results of sterility tests of seven...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Getinge CM320 Series Washer Disinfector - Product Usage: A multi Recalled by...
The Issue: The potential that the plastic inlet hose connections may deform or break as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by...
The Issue: There were customer reports of separation between the tubing and Male Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended...
The Issue: Acetabular Liners have a higher than acceptable oxidation limit, potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Recalled by...
The Issue: Acetabular Liners have a higher than acceptable oxidation limit, potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....
The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERF Novae Dual Mobility Cup Insert 47/28- ApeX-LNK Poly Liner. Recalled by...
The Issue: Acetabular Liners have a higher than acceptable oxidation limit, potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...
The Issue: Shipping box may contain wrong model.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...
The Issue: Misleading error messages and a gap in the Operator Manual which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...
The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...
The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.