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. 2,571 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,571 in last 12 months

Showing 1804118060 of 49,976 recalls

Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.32 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 128" (325 cm) Appx 16.6 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 2.8 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· Sysmex America, Inc.

Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...

The Issue: Insufficient amount of antibody without an error message or alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· OrthoPediatrics Corp

Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...

The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2020· Dynex Technologies, Inc.

Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...

The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...

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

Class II — Potential Health HazardOngoing
DrugJuly 3, 2020· Granules Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by Granules...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· AAA Cosmetica, SA de CV

Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...

The Issue: Chemical Contamination: Product contains methanol.

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Sildenafil 50 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 300 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Yohimbine HCL 5.4mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund