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. 896 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
896 in last 12 months

Showing 45061–45080 of 46,762 recalls

Medical DeviceSeptember 7, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw...

The Issue: This action is being initiated following a detailed investigation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Instrumentation Industries Inc

Recalled Item: Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators...

The Issue: Firm initiated an update to Directions for Use necessitating replacement of...

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

Class II — Potential Health HazardOngoing
DrugSeptember 6, 2012· Church & Dwight Inc

Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...

The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/2" Diced Yellow Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/4" Slivered Yellow Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Eco Health, Inc.

Recalled Item: florAlign Prebiotic Formula Recalled by Eco Health, Inc. Due to Potential...

The Issue: Eco Health is recalling florAlign Prebiotic Formula because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 1/4" Diced Red Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 6, 2012· Gills Onions, LLC

Recalled Item: 3/16" Slivered Red Onions Recalled by Gills Onions, LLC Due to Potential...

The Issue: Gills Onions is recalling diced and slivered onions because it may be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0 w/Needles with Orthocord Product Number: 222968 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Screw Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Fracture...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Recalled...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· Gynex Corporation

Recalled Item: Sterile Recalled by Gynex Corporation Due to The wrong electrical connector...

The Issue: The wrong electrical connector pin was attached to the cord during assembly...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Ethibond without needles Product Number: 222964 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Recalled...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing