Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 2614126160 of 27,254 recalls

Medical DeviceSeptember 17, 2012· KCI USA, Inc.

Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...

The Issue: KCI has issued a medical device correction for the BariAir Therapy System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2012· Ge Healthcare It

Recalled Item: Centricity PACS System versions 3.X and higher and 4.X and Recalled by Ge...

The Issue: There is a potential loss of image(s) associated with the Centricity to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular AB Shells with Holes. The Trilogy Acetabular System...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Sorin Group USA, Inc.

Recalled Item: Gish 3/8 x 3/8" Straight Connector with Luer fitting Recalled by Sorin Group...

The Issue: Due to a molding irregularity, certain lots of connectors have the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy F/M Acetabular Shell without holes SOLID HA. Several ODs: 38MM...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Creatinine 120 CP Recalled by Horiba Instruments, Inc dba Horiba...

The Issue: This recall was initiated because some customers were experiencing an alarm...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM Recalled by...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shell Spiked. The Trilogy Acetabular System is indicated...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular AB Shells with Cluster Holes. The Trilogy Acetabular...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Hologic, Inc.

Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight2 Recalled by Hologic, Inc....

The Issue: InSight2, version 4.0 and 4.0.1 - DICOM images stored in PACS may be flipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: Minotrol 16 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: HORIBA Medical Irvine Technical Support received reports from some customers...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Hologic, Inc.

Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...

The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Advandx Inc

Recalled Item: AdvanDx E. coli/P. aeruginosa PNA FISH Recalled by Advandx Inc Due to...

The Issue: Some strains of Pseudomonas putida cross-react with the P. aeruginosa PNA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy F/M Acetabular Shell with Uni-Hole. The Trilogy Acetabular System...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Advandx Inc

Recalled Item: AdvanDx GNR Traffic Light PNA FISH Recalled by Advandx Inc Due to GNR...

The Issue: GNR Traffic Light PNA Fish may have false positive results with Pseudomonas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Sorin Group USA, Inc.

Recalled Item: Gish 3/8 x 1/2" Reducer Connector with Luer fitting Recalled by Sorin Group...

The Issue: Due to a molding irregularity, certain lots of connectors have the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shell with Cluster Holes. The Trilogy Acetabular System...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Modular Stem Recalled by Zimmer, Inc. Due to Zimmer Inc. is initiating a...

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· 3M Company - Health Care Business

Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...

The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...

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

Class II — Potential Health HazardOngoing