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. 2,571 recalls have been distributed to Oklahoma in the last 12 months.
Showing 17781–17800 of 49,976 recalls
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVANOS MIC-KEY SF Gastrostomy Feeding Tube Recalled by Avanos Medical, Inc....
The Issue: Devices had cracked or detached from the feeding tube body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare Recalled by RAYSEARCH LABORATORIES AB Due to When performing offline...
The Issue: When performing offline image review in RayCare 2C, RayCare 3A and RayCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooked Recalled by Kader Exports Pvt. Ltd. Due to Potential Salmonella...
The Issue: Frozen cooked shrimp is possibly contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Control Recalled by Medline Industries Inc Due to Product was shipped with...
The Issue: Product was shipped with (ice) instead of frozen (dry ice).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to Chemical Contamination:...
The Issue: Chemical Contamination: HERBACIL, Antiseptic Hand Sanitizer, 70% Alcohol,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to CGMP Deviations:...
The Issue: CGMP Deviations: products were recalled because they were manufactured in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine 15mg grey/Yellow Capsules Recalled by Calvin Scott & Company,...
The Issue: CGMP Deviations: Light sensitive drug products repackaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrochlorothiazide 25mg tablets Recalled by Calvin Scott & Company, Inc....
The Issue: CGMP Deviations: Light sensitive drug products repackaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine HCL Blue/Clear capsules Recalled by Calvin Scott & Company, Inc....
The Issue: CGMP Deviations: Light sensitive drug products repackaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.