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. 1,057 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,057 in last 12 months

Showing 9681–9700 of 27,254 recalls

Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· ROi CPS LLC

Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...

The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Nextremity Solutions

Recalled Item: InCore Lapidus Disposable Kit 28mm Left Recalled by Nextremity Solutions Due...

The Issue: Product could potentially contain an undersized inner diameter of the 40mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Nextremity Solutions

Recalled Item: InCore Lapidus Disposable Kit 28mm Right Recalled by Nextremity Solutions...

The Issue: Product could potentially contain an undersized inner diameter of the 40mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: InterV CurvePlus Kit Recalled by Zavation Due to Products distributed as...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Unipedicular Bone Access Kit with Drill Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Unipedicular Cement Delivery Cannula Kit Recalled by Zavation Due...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Bevel Tip Trocar Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET (1 X DIAMOND 1 X Recalled by Zavation Due...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT ACCESS DIAMOND TIP Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION STERILE. For use in Recalled by...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: InterV Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: OsteoFlex Cement and Mixing System Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing