Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,510 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,510 in last 12 months

Showing 2640126420 of 28,334 recalls

Medical DeviceMarch 22, 2013· Lighthouse For The Blind

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.

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...

The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

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.

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

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.

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

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.

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2013· Philips Medical Systems (Cleveland) Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2013· Biomet U.K., Ltd.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2013· Horiba Instruments, Inc dba Horiba Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2013· Beckman Coulter Inc.

Recalled Item: AU5800 Clinical Chemistry Analyzer The Beckman Coulter AU5800 Clinical...

The Issue: Beckman Coulter, Inc. initiated this recall because there is a software...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Accuray Incorporated

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...

The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

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.

Class II — Potential Health HazardOngoing