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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 2782127840 of 49,976 recalls

Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
FoodOctober 19, 2017· Market America Inc

Recalled Item: bliss anti-stress formula Dietary Supplement Recalled by Market America Inc...

The Issue: Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2017· Teleflex Medical

Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...

The Issue: Teleflex is recalling these products because the jaws of the tool tip may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Siemens Healthcare Diagnostics

Recalled Item: BC Thrombin Reagent Kit Lot Number 46751 Recalled by Siemens Healthcare...

The Issue: The BC Thrombin Reagent kit lot 46751 (contains Thrombin Reagent lot 517468)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing