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. 2,580 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15721–15740 of 49,976 recalls
Recalled Item: Delflex Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...
The Issue: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panera Lobster Bisque Recalled by Blount Fine Foods Corporation Due to...
The Issue: Lobster bisque contains undeclared noodle with egg ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Freshness Guaranteed Macaroni Salad Amish Recalled by Reser's Fine Foods,...
The Issue: Undeclared Wheat and/or Egg. The bottom label of Macaroni Salad Amish was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...
The Issue: Barcode label extended expiration date. Barcode located at the short side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E3800 PC Units (spare parts) Recalled by Radiometer Medical ApS Due to Due...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to specimens...
The Issue: specimens collected in transport media may result is false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trader Joe's Restaurant Style White Corn Tortilla Chips Recalled by Snak...
The Issue: White Corn Tortilla Chips may contain undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...
The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...
The Issue: Defective container; syringe content migrating past the seal of the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by an ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...
The Issue: The firm was notified by its ingredient supplier of Medium Chain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 30 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO AB Recalled by DJ Orthopedics de Mexico S.A. de C.V....
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY PRO Recalled by DJ Orthopedics de Mexico S.A. de C.V. Due to failed...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.