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. 2,379 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,379 in last 12 months

Showing 4642146440 of 49,976 recalls

Medical DeviceApril 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...

The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...

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

Class II — Potential Health HazardOngoing
DrugApril 19, 2013· Novartis Consumer Health

Recalled Item: Lamisil AT (terbinafine hydrochloride cream 1% antifungal) Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...

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

Class III — Low RiskOngoing
Refund
DrugApril 19, 2013· Qualitest Pharmaceuticals

Recalled Item: GLIMEPIRIDE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: One oversized tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2013· Ge Healthcare It

Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...

The Issue: GE Healthcare has become aware of a potential data loss issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2013· Sandoz Incorporated

Recalled Item: Amoxicillin Capsules USP 500 mg Recalled by Sandoz Incorporated Due to...

The Issue: Presence of Foreign Substance, Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...

The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2013· BioMerieux SA

Recalled Item: VIDAS D-Dimer Exclusion II Recalled by BioMerieux SA Due to Customer...

The Issue: Customer complaints about not repeatable results below the detection limit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM KIT Recalled by DePuy Spine, Inc. Due to...

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Recalled by DePuy Spine, Inc. Due to...

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· DePuy Spine, Inc.

Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 11CC PLUS KIT Recalled by DePuy Spine, Inc....

The Issue: During injection of cement, the water in the hydraulic pump leaks past the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Alcon Grieshaber AG

Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...

The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LX System(s) and UniCel DxC 600/800 System(s) Lactate Reagent...

The Issue: Beckman Coulter initiated the recall for the Lactate Assay (LACT) Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Ziemer Usa Inc

Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...

The Issue: A defect in the controller board can lead to the condenser to the video...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Alere San Diego, Inc.

Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...

The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...

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

Class II — Potential Health HazardOngoing