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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2124121260 of 46,762 recalls

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: VANTEX 7FR 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: PORT AND IO ACCESS DRESSING KIT DT15780A 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: CENTRAL LINE BUNDLE ECVC6375 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: IV KIT - SORBAVIEW IVS3475 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: CAP BUNDLE KIT DYNDC2137 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: PEDIATRIC PICC INSERTION TRAY CVI4450 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 VENOUS ACCESS DEVICE BUNDLE ECVC2840 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
DrugApril 23, 2019· D.B.P. Distribution

Recalled Item: Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 23, 2019· Akorn Inc

Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...

The Issue: Failed impurities/degradation specification: Out of Specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 23, 2019· Stryker Corporation

Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...

The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC Kit Product Code: ASK 45541 LVH1 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V Recalled by CooperSurgical, Inc. Due...

The Issue: 2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC Kit Product Code: ASK 45541 RWJ4 Recalled by Arrow International...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing