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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 2170121720 of 49,976 recalls

DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Walgreens Sodium Chloride Ophthalmic Solution Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: OCuSOFT Tetravisc Tetracaine HCl 0.5% Sterile Anesthetic Single Dose 0.6 mL...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Altaire Sterile Eye Wash Recalled by Altaire Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Altacaine (Tetracaine Hydrochloride) Ophthalmic Solution Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8...

The Issue: Failed Impurities/Degradation Specifications: Kaitlib Fe Tablets has an out...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...

The Issue: The firm conducted internal investigations that confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Qiagen Sciences LLC

Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...

The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Privapath Diagnostics Ltd

Recalled Item: Universal Sexual Health Testing Kit Recalled by Privapath Diagnostics Ltd...

The Issue: A supplier informed PrivaPath Diagnostics that there is a potential for...

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

Class II — Potential Health HazardOngoing