Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,375 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,375 in last 12 months

Showing 2688126900 of 27,645 recalls

Medical DeviceJune 29, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module model 8100. Subsequent product code: FPA The Recalled by...

The Issue: The recall was initiated because Carefusion identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Encore Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Sara Plus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· C.R. Bard, Inc., Urological Division

Recalled Item: Bard Foley procedural trays packaged in breather bags. The product Recalled...

The Issue: Incomplete seal on sterile packages of product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DGXN Slides --- [REF] 834 3386. Product Recalled...

The Issue: Ortho Clinical Diagnostics revised the VITROS Chemistry Products DGXN Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· Advanced Sterilization Products

Recalled Item: STERRAD Cyclesure Biological Indicator (BI) Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling certain lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Mar Cor Purification

Recalled Item: Mar Cor Purification CWP Reverse Osmosis System. Models 101 Recalled by Mar...

The Issue: There exists a potential situation with the crimp connection at the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· KCI USA, Inc.

Recalled Item: RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention...

The Issue: The firm is initiating a voluntary medical device correction for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Perkinelmer

Recalled Item: Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010...

The Issue: Contamination from GSP Shaker unit results in decreased signal activity of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE 3 Blood and Fluid Warmer Recalled by Smiths Medical...

The Issue: HOTLINE 3 Blood and Fluid Warmer( Reorder No. HL-390 ) disposable is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Sunrise Medical (US) LLC

Recalled Item: Padded Swing Away Arm Rest with Receiver Recalled by Sunrise Medical (US)...

The Issue: Reports of injury when the Padded Swing Away Armrest is used for full body...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Bridgepoint Medical

Recalled Item: BridgePoint Medical Recalled by Bridgepoint Medical Due to BridgePoint...

The Issue: BridgePoint Medical Inc. is voluntarily recalling Stingray Catheter, Model...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece...

The Issue: Disposable T-Piece circuits used with resuscitation systems are unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

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

Class II — Potential Health HazardOngoing