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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 2720127220 of 49,976 recalls

Medical DeviceJanuary 11, 2018· Ellex iScience, Inc.

Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...

The Issue: Sterility failure found in one of the units in the lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2018· Riverpoint Medical, LLC

Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...

The Issue: Product is labeled with "CE", but is not yet approved in the European Union.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 5, 2018· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit for In Vitro Recalled...

The Issue: Contains a gel-like contaminant that may affect product performance.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 5, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis angiographic x-ray system Recalled by Siemens Medical Solutions...

The Issue: Certain systems may have leaking of the plastic coolant couplings, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2018· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Recalled by...

The Issue: Contains a gel-like contaminant that may affect product performance.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2018· Toshiba American Medical Systems Inc

Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...

The Issue: The power supply unit may be damaged and may fail to start up when the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...

The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 4, 2018· Ventura Foods Llc

Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy

The Issue: SunGlow contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2018· Dollar General Corporation, Inc.

Recalled Item: Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT...

The Issue: The firm received Ice Oatmeal Cookies that actually contain Coconut Macaroon...

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

Class I — Serious Health HazardOngoing
Refund