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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5381–5400 of 28,654 recalls
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Product Code 6802413 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Product Code 6802783 and Product...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stay Safe Cap Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Updating the labeling to include additional warnings and contraindications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...
The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to This recall is...
The Issue: This recall is part of a 2-issue recall for the same system. When using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.