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. 933 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
933 in last 12 months

Showing 48701–48720 of 49,976 recalls

FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Pumpkin Spice Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Chocolate Peanut Butter Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Vanilla Maple Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Coffee Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Chocolate Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Arctic Zero, Inc.

Recalled Item: Chocolate Dipped Bars Recalled by Arctic Zero, Inc. Due to Undeclared Milk

The Issue: Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2012· Combs Produce

Recalled Item: Round Fresh Tomatoes sold in bulk boxes Recalled by Combs Produce Due to...

The Issue: The product has the potential to be contaminated with E. coli 0157: H7.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2012· Ben Venue Laboratories Inc

Recalled Item: Leucovorin Calcium Injection USP Recalled by Ben Venue Laboratories Inc Due...

The Issue: Presence of Particulate Matter: visible crystalline particulates and the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2012· Southwind Foods LLC dba Great American Seafood Imports Co.

Recalled Item: Great American Seafood Imports Co. Cooked Shrimp Meat. Size: 300/500...

The Issue: Southwind is recalling cooked shrimp meat because it contains undeclared red...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: The ABL software version 6.12 for the ABL800 analyzer. The Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Kimberly-Clark Corporation

Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...

The Issue: Package seam of some units may not remain properly sealed to ensure the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Kimberly-Clark Corporation

Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...

The Issue: Package seam of some units may not remain properly sealed to ensure the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Stryker Spine

Recalled Item: Aviator Drill Bit (10 mm Recalled by Stryker Spine Due to Aviator drill bits...

The Issue: Aviator drill bits are 10 mm longer than the Hybrid drill bits and are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: The ABL software version 6.12 for the ABL800 and ABL700 Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· OPTI Medical Systems, Inc

Recalled Item: BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are Recalled by...

The Issue: The values reported for PCO2 by BP7561 B-Lac cassettes are biased at high...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white...

The Issue: Distal part of the anchor may break on insertion into bone during surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545...

The Issue: Three complaints have been filed where the Hoffman LRF Telescopic Struts...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures...

The Issue: Distal part of the anchor may break on insertion into bone during surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Chicago X-Ray Systems, Inc.

Recalled Item: Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is Recalled by...

The Issue: The IntraOs 70 system was found to have missing or incomplete system labels...

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

Class II — Potential Health HazardOngoing