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. 2,449 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,449 in last 12 months

Showing 3616136180 of 49,976 recalls

Medical DeviceNovember 5, 2015· Brainlab AG

Recalled Item: RT Elements are applications for radiation treatment planning for use...

The Issue: Large objects with fine resolution are potentially displayed cropped when...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2015· CareFusion 303, Inc.

Recalled Item: Alaris Pump SmartSite Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2015· Brainlab AG

Recalled Item: RT Elements are applications for radiation treatment planning for use...

The Issue: Large objects with fine resolution are potentially displayed cropped when...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2015· Ormco/Sybronendo

Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...

The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2015· Edwards Lifesciences, LLC

Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP Cookies GINGER ZINGER GLUTEN FREE Recalled by Tate's...

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP CHOCOLATE CHIP COOKIES Recalled by Tate's Wholesale, Llc....

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing