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.
Showing 26681–26700 of 28,654 recalls
Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner & Reprocessor System Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) has determined that a limited number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: If the operator selects a patient name from the worklist using the mouse and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...
The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...
The Issue: Investigation of complaints found excessive use of the instrument could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.