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 17761–17780 of 49,976 recalls
Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...
The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...
The Issue: Device did not meet the updated EUA packet requirements for positive percent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized Recalled by...
The Issue: Undeclared cashews in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint Recalled by...
The Issue: Undeclared cashews in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint sized Recalled...
The Issue: Undeclared cashews in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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 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: 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: 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: 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 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: 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.