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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26561–26580 of 28,654 recalls
Recalled Item: Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103...
The Issue: Alpine Biomed ApS is recalling Natus neurology Dantec KEYPOINT.NET ver. 2.20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an...
The Issue: Several complaints were recorded regarding one of the three screws driving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Electrosurgery Probe Plus II Recalled by Ethicon Endo-Surgery Inc...
The Issue: The firm is recalling the ENDOPATH Probe Plus II Shafts because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defribillator Recalled by Philips Healthcare Inc. Due...
The Issue: Device may fail to deliver defibrillation therapy in either Manual Defib or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac Recalled...
The Issue: Newport Medical Instruments is conducting a voluntary recall on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...
The Issue: Review of validation information and customer complaints which indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas¿ 8000 modular analyzer series software version 03-01 Recalled by Roche...
The Issue: When using the cobas e 602 module, Diluent Multiassay may be used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExoShape Soft Tissue Fastener 12 mm x 30 mm by Medshape Solutions, INC. Due...
The Issue: Expiration date on the patient label and date on the product carton were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...
The Issue: Software update to fix multiple safety related issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...
The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...
The Issue: Internal investigation demonstrated under-recovery for glucose when tested...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.