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. 1,076 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
1,076 in last 12 months

Showing 14281–14300 of 49,976 recalls

Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor with software VD12- angiography systems developed for Recalled...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Biomeme, Inc.

Recalled Item: Biomeme SARS-CoV-2- Real Time RT-PCR Test Recalled by Biomeme, Inc. Due to...

The Issue: The current IFU specifies a shelf-life of one week after resuspension of the...

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

Class II — Potential Health HazardOngoing
FoodOctober 20, 2021· ProSource Produce LLC

Recalled Item: Whole raw WHITE onions are imported from Chihuahua of MEXICO. Recalled by...

The Issue: Salmonella Oranienburg.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 20, 2021· ProSource Produce LLC

Recalled Item: Whole raw YELLOW onions are imported from Chihuahua of MEXICO. Recalled by...

The Issue: Salmonella Oranienburg.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 20, 2021· ProSource Produce LLC

Recalled Item: Whole raw RED onions are imported from Chihuahua of MEXICO. Recalled by...

The Issue: Salmonella Oranienburg.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Failed Stability Specifications: Out-of-specification results observed in a...

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

Class III — Low RiskOngoing
Refund
DrugOctober 19, 2021· Teligent Pharma, Inc.

Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Defective Container

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2021· MERCK SHARP & DOHME CORP

Recalled Item: Cubicin (daptomycin for injection) Recalled by MERCK SHARP & DOHME CORP Due...

The Issue: Presence of Particulate Matter: Identified as Glass Particles

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 19, 2021· Teligent Pharma, Inc.

Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Defective Container

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2021· InfuTronix LLC

Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...

The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2021· Medtronic Neuromodulation

Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...

The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...

The Issue: A potential risk for false negative nitrite results exists when endogenous...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 15, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...

The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti-HBc IgM Controls Recalled by...

The Issue: Ortho Clinical Diagnostics confirmed a complaint that some VITROS...

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

Class III — Low RiskOngoing
Medical DeviceOctober 15, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...

The Issue: During stent graft deployment, the spindle may detach from the distal end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...

The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...

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

Class II — Potential Health HazardOngoing