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 14661–14680 of 28,654 recalls
Recalled Item: NeuViz 128 Multi-slice CT Scanner System with software version...
The Issue: For surview scan length more than 500mm,if the user aborts or skips the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...
The Issue: An internal assessment of packaging confirmed the potential for a breach in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insufflation tubing to be used with varies insufflator units. Recalled by...
The Issue: The sterile single-use tubing may contain higher ethylene oxide (EO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVE 2 Birthing Bed Recalled by Linet Spol. S.r.o. Due to LINET has recently...
The Issue: LINET has recently become aware of a potential safety issue for the AVE 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...
The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.