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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26921–26940 of 49,976 recalls
Recalled Item: M&P Food Productions brand Vareniki Recalled by M & P Food Productions, Ltd....
The Issue: Product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: M&P Food Productions brand Hand Made Russian Style Blintzes Recalled by M &...
The Issue: Product contains undeclared wheat and undeclared FD&C Red #40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: M&P Food Productions brand Vareniki Sour Cherry Recalled by M & P Food...
The Issue: Product contains undeclared wheat and Red #40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: M&P Food Productions brand Hand Made Russian Style Blintzes Recalled by M &...
The Issue: Product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 0.9% Sodium Chloride Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: Customer complaint of particulate matter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doyen-Collin Mouth Gag 120MM/ General Instruments Recalled by Aesculap...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic ADT1018 Flow QC Clear Advantage Tubing Recalled by Transonic...
The Issue: The sterility of the device cannot be assured. There is a potential for an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Following a period of inactivity, the mass storage device may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g Recalled by...
The Issue: The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce &...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PVP Scrub Solution Recalled by Medline Industries Inc Due to Subpotent Drug:...
The Issue: Subpotent Drug: product not meeting the iodine assay level requirements...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...
The Issue: Microbial contamination of Non-Sterile Product; product contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ONCOR Avant-garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M2 / PRIMUS Mid-Energy Recalled by Siemens Medical Solutions USA,...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI Recalled by Siemens Medical Solutions USA, Inc Due to Control...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Expression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...
The Issue: The duodenoscopes are being recalled in order to replace the forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.