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. 1,679 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,679 in last 12 months

Showing 4546145480 of 47,764 recalls

Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: Microplate Recalled by Perkinelmer Due to Truncated V-Bottomed Microplate...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Dako Denmark A/S

Recalled Item: CoverStainer Slide Rack The CoverStainer Slide Rack is an accessory Recalled...

The Issue: The expected life time of the CoverStainer slide racks (CS 10330) does not...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2012· Pfizer Inc.

Recalled Item: TORISEL Kit (temsirolimus) injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential that a low level of endotoxins may...

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

Class III — Low RiskOngoing
Refund
FoodNovember 23, 2012· Newman'S Own Inc.

Recalled Item: Newman's Own Lite Honey Mustard Dressing Recalled by Newman'S Own Inc. Due...

The Issue: Newman's Own Lite Honey Mustard Dressing was labeled with an incorrect back...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.

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

Class III — Low RiskOngoing