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. 2,553 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,553 in last 12 months

Showing 1924119260 of 49,976 recalls

DrugJanuary 28, 2020· Teva Pharmaceuticals USA

Recalled Item: Tramadol Hydrochloride Tablets USP CIV Recalled by Teva Pharmaceuticals USA...

The Issue: Labeling: Incorrect package insert - Patient leaflets for the specified lots...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2020· Graviti Pharmaceuticals Private Limited

Recalled Item: Atorvastatin Calcium Tablets Recalled by Graviti Pharmaceuticals Private...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that one 20 mg...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Cheddar Garlic Biscuits Recalled by Southern...

The Issue: Undeclared allergen: Wheat Undeclared colors: Yellow #5 and #6.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Apple Crisp mix Recalled by Southern Sisters...

The Issue: Undeclared allergen: Pecans

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Butter Pecan Cheeseball mix Recalled by Southern...

The Issue: Undeclared allergens: Milk, Wheat, Soy, and Almond.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Shrimp and Stone-Ground Grits Recalled by Southern...

The Issue: Undeclared allergen: Milk. Undeclared colors: Yellow #5 and #6.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Taco Soup Recalled by Southern Sisters Gourmet Due...

The Issue: Undeclared allergens: Milk and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Crab Cake Mix Recalled by Southern Sisters Gourmet...

The Issue: Undeclared allergens: Wheat and Soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Oven Fried Chicken Recalled by Southern Sisters...

The Issue: Undeclared allergen: Wheat

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2020· Southern Sisters Gourmet

Recalled Item: Southern Sisters Gourmet Caramel Apple Cobbler Recalled by Southern Sisters...

The Issue: Undeclared allergen: Wheat

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2020· Smith & Nephew, Inc.

Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...

The Issue: The spike rail was manufactured with an oversized thru-hole which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Smith & Nephew, Inc.

Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...

The Issue: The spike rail was manufactured with an oversized thru-hole which could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medicrea International

Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...

The Issue: An internal component was assembled in the incorrect orientation, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Qiagen Sciences LLC

Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...

The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medicrea International

Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...

The Issue: An internal component was assembled in the incorrect orientation, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medtronic, PLC

Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...

The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Breas Medical, Inc.

Recalled Item: Protective Cover Vivo 55/65 (Used for Vivo 50/65) Recalled by Breas Medical,...

The Issue: The outlet hole of the exhalation valve control pressure tube on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...

The Issue: CGMP deviations: Product bottle may be absent of desiccant.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...

The Issue: CGMP deviations: Product bottle may be absent of desiccant.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund