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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,480 in last 12 months

Showing 2578125800 of 49,976 recalls

Medical DeviceJuly 3, 2018· Radiometer America Inc

Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...

The Issue: The analyzer software may cause a mis-match of patient demographics and test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Abbott Vascular

Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...

The Issue: Incorrect expiration being entered for one lot.

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2018· Byrd Cookie Co

Recalled Item: PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES Recalled by Byrd Cookie Co Due...

The Issue: Red 40 & Red 3 were not listed in the ingredients statement

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 2, 2018· Hudson Scientific LLC

Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...

The Issue: The device and its accessories may not have been manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Water Pik, Inc.

Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...

The Issue: Charging base may overheat with localized melting and sparking, possibly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Cypress Medical Products LLC

Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...

The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial Recalled...

The Issue: Presence of Particulate Matter: identified as glass and silicone material

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 2, 2018· Radiometer America Inc

Recalled Item: Product: ABL800 FLEX with Crea. The ABL800 with Crea is Recalled by...

The Issue: From three incidents in Denmark and Sweden, comparison studies on patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Luminex Corporation

Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...

The Issue: An incorrect control board and firmware installed in some of the Hand Held...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: If the beam model has a highly asymmetric primary source, it is not...

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

Class II — Potential Health HazardOngoing