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

46,762 total recalls
987 in last 12 months

Showing 20941–20960 of 46,762 recalls

Medical DeviceMay 28, 2019· Medline Industries Inc

Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...

The Issue: Loose silicone particulate was found to be present on the shaft of the...

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

Class II — Potential Health HazardOngoing
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Pyrophosphate Kit Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2019· Synthetopes Inc

Recalled Item: Pentreotide (10 uGm) Recalled by Synthetopes Inc Due to Lack of Processing...

The Issue: Lack of Processing Controls.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 24, 2019· LAIRD SUPERFOOD INC

Recalled Item: Performance Mushrooms product is dried mushroom blend of 4 different...

The Issue: The product is incorrectly labeled with 14 mg of Iron and 78% DV when the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing