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. 1,050 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16341–16360 of 49,976 recalls
Recalled Item: CV Basin Set Pack Recalled by DeRoyal Industries Inc Due to Sternum saw...
The Issue: Sternum saw blades within procedure packs are not sterile. The surgical saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Pack Recalled by DeRoyal Industries Inc Due to Sternum saw blades...
The Issue: Sternum saw blades within procedure packs are not sterile. The surgical saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Heart Pack Recalled by DeRoyal Industries Inc Due to Sternum saw blades...
The Issue: Sternum saw blades within procedure packs are not sterile. The surgical saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: "Wildtree***Leslies Chili Blend***Organic & Gluten Free***Net Wt. 3.7 oz....
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: O Organics Plant Based Mushroom and Veggie Organic Burger Patties Recalled...
The Issue: Labeling error caused product to claim Gluten Free and Vegan when it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Wildtree***Taco Seasoning***Organic & Gluten Free***Net Wt. 8...
The Issue: Spice mixes contain undeclared gluten due to contaminated ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...
The Issue: CGMP Deviations: Individual Unidentified impurities results of the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...
The Issue: Superpotent Drug. Lidocaine higher concentration than listed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RUFFLES "PARTY SIZE" ORIGINAL POTATO CHIPS 13 1/2 oz. Recalled by Frito-Lay,...
The Issue: Potential to contain undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...
The Issue: Retail Box did not contain list of ingredients or allergen statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...
The Issue: On January 7, 2021, STERIS identified that the glued bond between the beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.