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 16741–16760 of 28,654 recalls
Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...
The Issue: May produce erroneously low results from specific well sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: Broken or missing screws and retaining clips. This may be due to screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...
The Issue: Customers may receive the incorrect size implant from what is labeled on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The device could have a missing spanner nut and snap ring which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....
The Issue: May contain endotoxin levels which have been confirmed to exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...
The Issue: The device may process the same sample with two different sample IDs and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...
The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Software issue with Center Beam in Field functionality. Issue can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...
The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...
The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.