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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 27181–27200 of 27,254 recalls
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Body X--ray Scanner This device is indicated as a Recalled by Toshiba...
The Issue: 1. It has been found that in raw data processing for Go&Return helical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC IT3000 Recalled by GE OEC Medical Systems, Inc Due to GE Healthcare...
The Issue: GE Healthcare Surgery had discovered that using the Inverted Headset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knife Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triage TOX Drug Screen Panel Recalled by Alere San Diego, Inc. Due to...
The Issue: Biosite is recalling the Triage TOX Drug Screen kits where the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Encompass The reporting site is using the Encompass software...
The Issue: Sunquest is recalling the Sunquest Encompass versions 2.4 and later because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Recalled by...
The Issue: The firm is initiating this recall because the implied or stated indications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnvatec SpA brand Diver C.E. Recalled by Invatec Llc Due to Devices labeled...
The Issue: Devices labeled for an intended use was not included in the existing 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that...
The Issue: Zynex notified customers that a malfunction in the IF 8000 can result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.