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. 2,617 recalls have been distributed to Oklahoma in the last 12 months.
Showing 11201–11220 of 28,654 recalls
Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Recalled by GE Healthcare, LLC Due to Rotor bearing screws were...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...
The Issue: Masks processed at one site were not maintained at levels of condensation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...
The Issue: Due to non-surgical isolation gowns not meeting all performance test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...
The Issue: The firm registered the product as a Class I device, but has since been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...
The Issue: Connector between support surface and pump may be out of tolerance resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.