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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 3990139920 of 46,762 recalls

Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Recalled by Davol,...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Mar Cor Purification

Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...

The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...

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

Class II — Potential Health HazardOngoing
DrugApril 23, 2014· Teva Pharmaceuticals USA

Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...

The Issue: Defective Delivery System; defective valve

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· C P Medical Inc.

Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...

The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...

The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Heraeus Kulzer, LLC.

Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...

The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· CareFusion 303, Inc.

Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...

The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...

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

Class I — Serious Health HazardOngoing
DrugApril 22, 2014· SigmaPharm Laboratories LLC

Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 22, 2014· Hamilton Medical, Inc.

Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....

The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 22, 2014· Biomet, Inc.

Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...

The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...

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

Class II — Potential Health HazardOngoing
DrugApril 21, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 21, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 21, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...

The Issue: Out of specification results for one of the two disinfectants.

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2014· Hospira Inc.

Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2014· Apotex Corp.

Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...

The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing