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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.
Showing 38261–38280 of 49,976 recalls
Recalled Item: SODIUM TETRADECYL (STERILE WATER) 30ML VIAL 2% INJECTABLE Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CYANOCOBALAMIN (PARABEN WATER) (10ML Recalled by Advanced Physician...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRADIOL CYPIONATE (SESAME OIL) 10ML Recalled by Advanced Physician...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLYCERIN (STERILE WATER) 100ML 71% INJECTABLE Recalled by Advanced Physician...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw...
The Issue: The Firebird Spinal Fixation System 6.5 mm x 55 mm Bone Screw, Self-Tapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...
The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...
The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...
The Issue: Vial to vial variation in the fill volume that could affect control recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...
The Issue: Complaints of the presence of artifacts that appears as small bead like...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure causing device inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure resulting in inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...
The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: measurements drawn on the 2nd and subsequent images of the series are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...
The Issue: Includes Information not stated in the intended use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...
The Issue: The intake port may be blocked which can cause the bag to fail to fill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...
The Issue: The pin which maintains the knob button, may disconnect and become lost....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corp. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Recalled by Mondelez...
The Issue: Fig Newtons brand Club Super Carton cookie products is mislabeled. The outer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...
The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEDASYS Computer-Assisted Personalized Sedation System Recalled by Ethicon...
The Issue: Ethicon has found that disinfecting methods not specified in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.