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. 2,251 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,251 in last 12 months

Showing 4508145100 of 46,762 recalls

Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 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 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 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 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· 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· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single...

The Issue: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...

The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Zimmer, Inc.

Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...

The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Premier Value Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Leader Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Wal-Mucil 100% Natural Fiber Recalled by Raritan Pharmaceuticals, Inc. Due...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Equate Fiber Therapy Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Berkley & Jensen Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc....

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Wal-Mucil Plus Calcium Fiber Capsules Recalled by Raritan Pharmaceuticals,...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Best Choice Health Care Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: CVS Pharmacy Fiber Capsules for Regularity Recalled by Raritan...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: DRxChoice Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund