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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.
Showing 41101–41120 of 49,976 recalls
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEW HOPE MILLS GLUTEN FREE CHIA PANCAKE & WAFFLE MIX Recalled by New Hope...
The Issue: New Hope Mills, Inc. has recalled New Hope Mills Gluten Free Chia Pancake...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Saba Shark Cartilage Complex Dietary Supplement Recalled by AMS Health...
The Issue: The product is being recalled due to the potential presence of Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.