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. 2,392 recalls have been distributed to Oklahoma in the last 12 months.
Showing 43661–43680 of 49,976 recalls
Recalled Item: Physique Enhancing Science ENHANCED Recalled by Physique Enhancing Science...
The Issue: Products contain "Aegeline" an unapproved New Dietary Ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile X-ray System Recalled by Shimadzu Medical Systems Due to Shimadzu...
The Issue: Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: During clinical operation, a malfunction may occur causing a system display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Failed Stability Specifications: this product is below specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crunch Pak Tart Apple Slices Recalled by Crunch Pak, LLC Due to Potential...
The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crunch Pak Natural Blue Raspberry Flavor Sliced Apples Recalled by Crunch...
The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crunch Pak Honeycrisp Apple Slices Recalled by Crunch Pak, LLC Due to...
The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crunch Pak Apple Slices with Low Fat Caramel Dip Recalled by Crunch Pak, LLC...
The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.