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 2768127700 of 49,976 recalls

Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Slit Knife: (a) Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· Pro-Med Instruments Gmbh

Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...

The Issue: The firm received reports of two breakages of the pin tips which occurred...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2017· Microline Surgical, Inc.

Recalled Item: ReNew Endocut Scissor Disposable Tip Recalled by Microline Surgical, Inc....

The Issue: Certain lots of disposable laparoscopic instrument tips may potentially have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...

The Issue: The internal configuration of the electrometers and the Real-Time control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2017· Microline Surgical, Inc.

Recalled Item: ReNew Dolphin Nose Disposable Dissector Tip Recalled by Microline Surgical,...

The Issue: Certain lots of disposable laparoscopic instrument tips may potentially have...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch Recalled by Aurora...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Chocolate Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Recalled...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund