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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16761–16780 of 28,654 recalls
Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...
The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...
The Issue: The recalling firm identified a software issue related to the Patient Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...
The Issue: Missing desiccant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...
The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...
The Issue: This Correction is being initiated based on a customer complaint received on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris MCK Onlay Insert Extractor. Recalled by Mako Surgical Corporation...
The Issue: Possible hinge pin disassociation from the Mako Onlay Insert Extractor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...
The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...
The Issue: Potential breakage of the endoscope s insertion tube bending section during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...
The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...
The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...
The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...
The Issue: A component used within the braking system may break resulting in one or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...
The Issue: Sterility failure found in one of the units in the lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...
The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.