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. 1,031 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,031 in last 12 months

Showing 13481–13500 of 27,254 recalls

Medical DeviceApril 29, 2019· Philips Ultrasound Inc

Recalled Item: Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0:...

The Issue: There is a potential that the image of one patient could get unexpectedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2019· KaVo Dental Technologies LLC

Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...

The Issue: The sensor's look up calibration files were incorrectly programmed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Cytocell Ltd.

Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...

The Issue: There is an error in the chromomap on the package insert.

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

Class III — Low RiskOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Inovo, Inc

Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...

The Issue: The pressure gauge (manometer) may dislodge from the threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· ASTRA, LLC

Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...

The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...

The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV START KIT IV8440 Recalled by Centurion Medical Products Corporation Due...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: INVASIVE PROCEDURE TRAY MNS9510 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC BUNDLE Recalled by Centurion Medical Products Corporation Due to Firm...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: INFUSA PORT KIT DYNDC1840E Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV SECUREMENT KIT IVS3405 Recalled by Centurion Medical Products Corporation...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CAP CHANGE KIT DYNDC1496B Recalled by Centurion Medical Products Corporation...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: STERILE CAP CHANGE KIT DYNDC1946B Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing