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. 936 recalls have been distributed to Oklahoma in the last 12 months.
Showing 44741–44760 of 49,976 recalls
Recalled Item: 6/16 oz. Chobani 0% Non-Fat Greek Yogurt Black Cherry Blended Recalled by...
The Issue: Greek yogurt product Chobani brand is recalled due to report of illnesses...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 0.5% Bupivacaine HCl and Epinephrine 1:200 Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility; potential for vial breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chocolate covered wafers (Bocadin) in plastic packaging sold under the...
The Issue: Undeclared Allergens (Milk): Mi Costenita BOCADIN wafer with chocolate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baxter CLEARLINK System Non-DEHP Three Lead Extension Set. 6.0" (15 cm)...
The Issue: The firm is issuing a voluntary recall due to the potential for pinholes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cranial Access (CRAK) Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra is recalling certain lots of Cranial Access Kit due to a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aldactone (spironolactone) tablets Recalled by Pfizer Us Pharmaceutical...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine Recalled by Novartis Consumer Health Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: The products are being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blanketrol III Recalled by Cincinnati Sub-Zero Products Inc Due to During a...
The Issue: During a label review it was discovered that both the Blanketrol III...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...
The Issue: Philips received reports from the field that the Flat Panel Detector (FPD)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1200 System Software: 1) V2.00 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creafuse Fruit Punch Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creafuse Grape Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GoPicnic Black Bean Dip & Plantain Chips Recalled by GoPicnic, Inc. Due to...
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.