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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 2062120640 of 28,654 recalls

Medical DeviceMarch 16, 2016· Terumo Medical Corporation

Recalled Item: PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath...

The Issue: Terumo Medical is initiating this recall due to complaints of valve leakage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Intuitive Surgical, Inc.

Recalled Item: da Vinci S Surgical System (IS4000) user manual English and Recalled by...

The Issue: Intuitive Surgical has found that the use of instruments other than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2016· Optovue, Inc.

Recalled Item: iVue and iVue 500 (now called iScan) OCT systems with Recalled by Optovue,...

The Issue: A software anomaly was detected that affects Optovue iVue and iVue 500 with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 for Proton Radiation Therapy Recalled by Mevion Medical Systems,...

The Issue: Possibility of Gantry Motion with Aperture or Compensator only partially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed w/o mattress & rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The vacuum suction...

The Issue: The vacuum suction tubing could be kinked within the machine resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed with mattress and rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Junction Boxes Recalled by Invacare Corporation Due to The firm recently...

The Issue: The firm recently identified a quality issue with the Junction box used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Ventlab LLC

Recalled Item: STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon...

The Issue: Stat-check CO2 indicators are non-functional. The indicator is yellow when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Recalled...

The Issue: New reprocessing instructions for the Olympus TJF-160/VF duodenoscopes,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...

The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV MST-30 Kit under the following labels: 1) 4F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV Introducer Kit under the following labels: 1) 4F...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing