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. 2,465 recalls have been distributed to Oklahoma in the last 12 months.
Showing 33241–33260 of 49,976 recalls
Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anasto AC Closure System and Anasto Universal Clip Remover- Anasto Recalled...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...
The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KC (Kill Cliff) Strawberries & Cream Protein Bars Recalled by Kill Cliff Due...
The Issue: Product may contain mold. Recall started on 6/21/16
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresh Express Kit Caesar salad Recalled by Fresh Express Incorpated Due to...
The Issue: The condiment kits in some Caesar Salad bags contain undeclared allergens:...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.