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

46,762 total recalls
950 in last 12 months

Showing 31821–31840 of 46,762 recalls

DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 10 mcg/mL HYDROmorphone HCl and 0.1% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 2 mcg/mL Fentanyl Citrate and 0.167% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 4 mcg/mL Fentanyl Citrate and 0.0625% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 0.125% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride Recalled...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· KVK-Tech, Inc.

Recalled Item: Benzphetamine Hydrochloride Tablets Recalled by KVK-Tech, Inc. Due to...

The Issue: Discoloration: presence of scuffing marks on tablets.

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

Class III — Low RiskOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2016· Brown & Haley Inc.

Recalled Item: Mountain Thins Trail Mix flavor Recalled by Brown & Haley Inc. Due to...

The Issue: Mountain Thins Trail Mix flavor, net wt. 5.3 oz., is recalled because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 4, 2016· NatureBox, Inc.

Recalled Item: Dark Cocoa Nom Noms 4.5oz. (128g) Recalled by NatureBox, Inc. Due to Firm...

The Issue: Firm was notified by third party warehouse that some Peanut Butter Nom Nom...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing