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. 2,443 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,443 in last 12 months

Showing 3696136980 of 49,976 recalls

DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Recalled...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: FML (fluorometholone ophthalmic ointment) 0.1% Recalled by Allergan Sales,...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: P.M. (Mineral Oil 42.5% and White Petrolatum 57.3%) Lubricant Recalled by...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: Rusch Flexi-slip tracheal tube Stylet Recalled by Teleflex Medical Due to...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Teleflex Medical

Recalled Item: R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip Recalled by...

The Issue: Due to reports of the plastic coating of the stylet splitting and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling

The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack with...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEPARIN Sodium in 0.45% Sodium Chloride Recalled by Cantrell Drug Company...

The Issue: Stability Data Does Not Support Expiry

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

Class II — Potential Health HazardOngoing
Refund