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. 2,485 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,485 in last 12 months

Showing 2278122800 of 28,654 recalls

Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Round Drain with Trocar Curved Trocar with Wound Recalled by Stryker...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· PhotoMedex, Inc.

Recalled Item: Iamin Moist Dressing and the Iamin Hydrating Gel: intended to Recalled by...

The Issue: The labeling for the Iamin family of medical devices (e.g. printed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Round Drain with Trocar Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Diamedix Corporation

Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...

The Issue: Product contained an incorrect substrate.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Olympus America Inc.

Recalled Item: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has...

The Issue: New and validated reprocessing procedures have been issued for the Olympus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 25, 2015· Lumenis Limited

Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....

The Issue: Device software treatment preset parameters for the XC treatment handpiece...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· CSA Medical

Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...

The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...

The Issue: Customer reports that the ventilator display can freeze. Ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· The Anspach Effort, Inc.

Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...

The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...

The Issue: Customers complained about under-recovery of non-Roche controls and...

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

Class II — Potential Health HazardOngoing