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. 2,520 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,520 in last 12 months

Showing 1790117920 of 28,654 recalls

Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 18"x22" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 18"x22" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x22" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x22" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 10"x15" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· ICU Medical Inc

Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to Potential for...

The Issue: Potential for the Connectivity Engine Module of the affected unit to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Custom Assemblies Inc

Recalled Item: Various custom surgical kits manufactured for CMS Recalled by Custom...

The Issue: The firm manufactured and distributed custom surgical kits which contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2017· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: ArjoHuntleigh Flowtron ACS900 Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: Reports of the device failure involving delivering continuous pressure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...

The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...

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

Class II — Potential Health HazardOngoing