Recalls distributed in Alaska
These notices name Alaska in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,282 stored notices name Alaska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Alaska too — those are in the archive.
Reported Sep 22, 2021
BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 15, 2021
Pipeline Flex Embolization Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc.,
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMimetic Therapeutics, LLC
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Aug 11, 2021
Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stanbio Laboratory, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 11, 2021
GlideScope Go Monitors
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunrise Medical (US) LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Chicken Street Taco kit in a plastic tray with a clear plastic lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Jun 9, 2021
Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Canada Company
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.