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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 14821–14840 of 49,976 recalls
Recalled Item: Zoll (IC-3893) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-4593) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...
The Issue: Nonconforming product was distributed in error. Product was nonconforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (SL-2593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-4593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-3893CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Stopcocks: (1) NAMIC STOPCOCK Recalled by Medline Industries Inc Due...
The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...
The Issue: Some devices may be associated with high and unexpected resistance to gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A800061 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A800360 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A319416AM Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A303416A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.