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. 2,078 recalls have been distributed to Oklahoma in the last 12 months.
Showing 6741–6760 of 28,654 recalls
Recalled Item: Titan Touch Scro Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain Gut Absorbable Sutures Recalled by Covidien, LP Due to Medtronic was...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Infrapubic 20 Cm Recalled by Coloplast Manufacturing US, LLC Due...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shanghai United Imaging Healthcare Co. Recalled by Shanghai United Imaging...
The Issue: Due to a software issue where the process of patient scanning, the scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...
The Issue: The external diameter of the biopsy instrument is larger than the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...
The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...
The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Re-optimization, after adding contours without forced density outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head Recalled by Zimmer, Inc. Due to Update the compatibility...
The Issue: Update the compatibility matrix as to in the Instructions for Use (IFU) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...
The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...
The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...
The Issue: Problem maintaining the stable placement of the battery may come loose from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...
The Issue: There have been complaints that the clip did not come out of the tube sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...
The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.