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 18821–18840 of 46,762 recalls

Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· TELEFLEX MEDICAL INC

Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...

The Issue: There is the potential for water to flood the column and enter the circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...

The Issue: Due to customer reports it has been determined that the inoculation system...

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

Class II — Potential Health HazardOngoing
DrugDecember 13, 2019· The Harvard Drug Group

Recalled Item: Memantine Hydrochloride Extended-release Capsules Recalled by The Harvard...

The Issue: Failed Dissolution Specifications: High out of specification result observed...

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

Class III — Low RiskOngoing
Refund
DrugDecember 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

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

Class III — Low RiskOngoing
Refund
FoodDecember 13, 2019· Wayfare Health Foods LLC

Recalled Item: Plant Based WayFare Vanilla Pudding Organic Dairy Free Recalled by Wayfare...

The Issue: Product recalled due to consumer complaints for bloating of package, off...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 13, 2019· Wayfare Health Foods LLC

Recalled Item: Plant Based WayFare Chocolate Pudding Organic Dairy Free Recalled by Wayfare...

The Issue: Product recalled due to consumer complaints for bloating of package, off...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 13, 2019· Wayfare Health Foods LLC

Recalled Item: Plant Based WayFare Butterscotch Pudding Organic Dairy Free Recalled by...

The Issue: Product is recalled due to consumer complaints for bloating of package, off...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: Clearlink System Continu-Flo Administration Sets Recalled by Baxter...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2019· Baxter Healthcare Corporation

Recalled Item: ONE-LINK Needle-free IV Connector Recalled by Baxter Healthcare Corporation...

The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- Uterine Sound 67465 STERILE SIMS UTERINE SOUND (83360) Y...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-Vaginal Speculum VS2000LST STERILE ER VAGINAL SPECULUM W/LIGHT...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- Port Draw Kit KNV30 PORT DRAW KIT Recalled by Centurion Medical...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- LC145 STERILE NICU LINE CHANGE KIT Recalled by Centurion Medical...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE Recalled by...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Recalled by Roche...

The Issue: Inability to dose the test strips, may result in a temporary inability to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- Biopsy Tray TRIBT170 BIOPSY TRAY Recalled by Centurion Medical...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-Suture Trays SUT10140 SUTURE TRAY SUT10290 LACERATION TRAY...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-Pelvic PE120 LARGE/MEDIUM PELVIC TRAY PE2200 PELVIC EXAM TRAY...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing