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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,431 in last 12 months

Showing 3884138860 of 49,976 recalls

Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the cable cart and the corrugated hose are unable to move freely, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· CooperSurgical, Inc.

Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...

The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP Recalled by...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 12, 2015· Stroheckers Inc Pharmacy

Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...

The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...

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

Class I — Serious Health HazardOngoing
Refund