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. 2,449 recalls have been distributed to Oklahoma in the last 12 months.
Showing 35281–35300 of 49,976 recalls
Recalled Item: 2.3mm Turbo-Power OTW Recalled by Spectranetics Corp. Due to The product is...
The Issue: The product is labeled with an expiration date that is past its shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....
The Issue: The device is reported to enter safe mode and is no longer able to charge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17...
The Issue: Hain Celestial Seasoning is recalling Celestial Seasonings Roastaroma Herbal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Buck's Fish Batter Mix Original Recalled by BlendTech Inc Due to...
The Issue: Product contains an undeclared milk ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BCS Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is...
The Issue: When a user performed radiography using the wireless FPD, a message window...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS XP Automated Blood Coagulation Analyzer System Recalled by Siemens...
The Issue: False short clotting times for PT on BCS and BCS XP with Dade Innovin can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: risperiDONE ORALLY DISINTEGRATING TABLETS Recalled by Zydus Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF...
The Issue: The Firm has discovered a Software bug.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21 Recalled by...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 Recalled by Resmed Corporation Due to Resmed Corporation is...
The Issue: Resmed Corporation is recalling Astral 100, 150 External Battery because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Estradiol Test Code E2 Catalog Number: K6463 Recalled...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number:...
The Issue: The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super Arrow-Flex Percutaneous Sheath Introducer Sets or CL-07635 Recalled by...
The Issue: Arrow has issued a recall for these products due to potential packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 71 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.