Recalls affecting Alaska
Notices that name Alaska in their distribution area, plus every nationwide recall — nationwide recalls reach Alaska too.
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Class II · 12 months ago
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class III · 12 months ago
Accriva Diagnostics, Inc. VerifyNow Prutest Platelet Reactivity Test REF 85225 Udi-Di recall: Due to an device without a premarket clearance being incorrectly package
Due to an device without a premarket clearance being incorrectly package and distributed.
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Class II · 12 months ago
Siemens Healthcare Diagnostics, Inc. Food Panel 3 Specific Allergen recall: The barcode orientation on affected devices causes incorrect scanning order
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 /…
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Class II · 12 months ago
Philips Respironics, Inc. SimplyGo Mini, Standard Battery Kit recall: Certain serial numbers of the SimplyGo Mini standard battery kit contain
Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose…
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Class I · 12 months ago
Medline Industries, LP Anesthesia Circuit Kits and other various kits that contain recall: Firm received multiple complaints of anesthesia circuit leaks due to cracks
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to…
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Class I · 12 months ago
Cerenovus Inc Cerepak Detachable Coil System - Name/REF: Uniform 2MM X 2.5 recall: Detachable coils system may fail to detach, which could result in hemorrhagic
Detachable coils system may fail to detach, which could result in hemorrhagic and ischemic stroke, procedural delays, or the need for additional…
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Class II · 12 months ago
Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class II · 12 months ago
Philips Medical Systems DMC GmbH Precision CRF recall: Philips has identified that some ceiling suspension telescopic carriages
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move…
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Class II · 12 months ago
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class II · 12 months ago
Medline Renewal LigaSure Small Jaw Instrument recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class II · 12 months ago
Philips Medical Systems DMC GmbH DigitalDiagnost C90 High Performance recall: Philips has identified that some ceiling suspension telescopic carriages
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move…
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Class II · 12 months ago
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class II · 12 months ago
Covidien Signia" Small Diameter Curved Tip Intelligent Reload recall: A manufacturing issue could lead to a malformed cover tube press
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the…
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Class II · 12 months ago
Medline Renewal LigaSure Blunt Tip Sealer/Divider recall: Medline Renewal has determined that certain areas on the device have
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and…
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Class II · 12 months ago
GE Healthcare Finland Oy Carescape ONE recall: Potential loss of monitoring on affected monitors when powered by certain
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and…
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Class II · 12 months ago
GE Healthcare Finland Oy B105P, B125P, B105M, B125M, B155M Patient Monitors recall: Potential loss of monitoring on affected monitors when powered by certain
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and…
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Class II · 12 months ago
Philips Medical Systems DMC GmbH Radiography 7300 C recall: Philips has identified that some ceiling suspension telescopic carriages
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move…
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Class II · 12 months ago
Olympus Corporation of the Americas Brand Name: Lithotriptor recall: The device may either fail to start up, or the transducer may start briefly
The device may either fail to start up, or the transducer may start briefly and then stop, accompanied by an error light on the generator. In…
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Class II · 12 months ago
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 recall: The nasal feeding tube may be occluded
The nasal feeding tube may be occluded
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Class I · 12 months ago
Lotus Vaping Technologies, LLC Monarch Premium Kratom Bali Gold powder is packaged recall: Product has the potential to be contaminated with Salmonella
Product has the potential to be contaminated with Salmonella
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Class I · 12 months ago
Lotus Vaping Technologies, LLC Monarch Premium Kratom Red Bali powder is packaged recall: Product has the potential to be contaminated with Salmonella
Product has the potential to be contaminated with Salmonella
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Class II · 12 months ago
Professional Botanicals, Inc. Product Name: Tense-X. Package: 175cc HDPE Bottle recall: Products contains Magnesium Salicylate
Products contains Magnesium Salicylate.
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Class I · 12 months ago
Lotus Vaping Technologies, LLC Monarch Premium Kratom White Elephant powder recall: Product has the potential to be contaminated with Salmonella
Product has the potential to be contaminated with Salmonella
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Class I · 12 months ago
Lotus Vaping Technologies, LLC Monarch Premium Kratom Green Maeng Da powder recall: Product has the potential to be contaminated with Salmonella
Product has the potential to be contaminated with Salmonella