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. 2,430 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,430 in last 12 months

Showing 1874118760 of 46,762 recalls

Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL NEEDLE COMPONENT AN-05505 Recalled by Arrow International Inc...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The potential exists for system movement to be permanently blocked by an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...

The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...

The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...

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

Class II — Potential Health HazardOngoing
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes Recalled...

The Issue: Potential to contain undeclared milk and coconut.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 19, 2019· Whole Foods Market

Recalled Item: 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes Net Wt Recalled...

The Issue: Potential to contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Randox Laboratories, Limited

Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...

The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...

The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...

The Issue: Potential issue associated with the instrument -end of the shaft could fail...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzymatic Creatinine (ECREA) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing