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. 2,326 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,326 in last 12 months

Showing 3354133560 of 46,762 recalls

Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2015· Pfizer Inc.

Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Superberry Maqui Camu - Sprouted Almond Spread. Product is packaged Recalled...

The Issue: Superberry Maqui Camu - Sprouted Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cinnamon Red Maca - Sprouted Almond Spread. Product is packaged in glass...

The Issue: Cinnamon Red Maca - Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cashew Cardamom - Sprouted Cashew Almond Spread. Product is packaged...

The Issue: Cashew Cardamom - Sprouted Cashew Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Coconut Cardamom - Sprouted Almond Spread. Product is packaged in glass jars...

The Issue: Coconut Cardamom- Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Hazelnut Raw Cacao - Sprouted Hazelnut Spread. Product is packaged in glass...

The Issue: Hazelnut Raw Cacao - Sprouted Hazelnut Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· JosNoe Medical, Inc.

Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...

The Issue: Damage to package seals potentially compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· 3M Company - Health Care Business

Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...

The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...

The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Partners In Medicine Llc

Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...

The Issue: Device non-conformity which may lead to an incorrect oscillometric...

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

Class II — Potential Health HazardOngoing