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. 2,361 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,361 in last 12 months

Showing 2342123440 of 46,762 recalls

FoodJuly 23, 2018· Pepperidge Farm, Incorporated

Recalled Item: Pepperidge Farm Goldfish Baked Snack Crackers Baked with Whole Grain...

The Issue: Pepperidge Farm has been notified by one of its ingredient suppliers that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2018· Johnson & Johnson Vision Care, Inc.

Recalled Item: Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear Recalled by...

The Issue: Johnson and Johnson Vision Care received a number of reports of a partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Qiagen Sciences LLC

Recalled Item: EZ1 Advanced XL Recalled by Qiagen Sciences LLC Due to An issue with the...

The Issue: An issue with the power branching printed circuit board (PCB) on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Tecan US, Inc.

Recalled Item: Freedom EV0-2 with any version of EVOware and EVOware Sample Recalled by...

The Issue: There is a software issue that can potentially impact sample identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Polyisoprene Condoms Recalled by Reckitt Benckiser LLC Due...

The Issue: The products failed the filed specification of 1.0kPa for Burst Pressure.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: EC20C 20G X 100CM CATH CLOSED Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TB19C CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFMHDT 17 GA X 4 FULL EPID KIT Recalled by B. Braun Medical, Inc. Due...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: GOVCE18TK ACCU-BLOC PERIFIX KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFPS PERIFIX FX CONT. EPID TRAY-LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFSA FULL TRAY W/17G TUOHY 19G SPRW Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CNB400TU3KUE 18GX4 CONTI THY ULTRA 360 Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TK CONT EPIDURALTUOHY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TKO PERIFIX ONE EPIDURAL FULL TRAY Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: ES1827KDS SPINAL/EPIDURAL FULL KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: ES1827K SPINAL/EPIDURAL TRAY (LF) Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18HKST CONT EPID 20G SOFTIP Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing