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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.

Medical devices

Reported Aug 8, 2012

The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2012

Frozen Oysters are packaged in 8 oz. 40 oz, and 3 lbs. The item numbers are 06413, 03777, FO/HS-OT8; 136300-20110430.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B & F, Inc., dba Hanmi, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2012

PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tripath Imaging, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2012

Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2012

superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

superDimension, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2012

TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2012

Olympic Cool-Cap System is intended to provide treatment for neonatal hypoxic-ischemic encephalopathy (HIE). The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natus Medical Incorporated

FDA (openFDA device enforcement)

Drugs

Reported Jun 27, 2012

Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distributed: Physicians Total Care, Inc., Tulsa…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physicians Total Care, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 20, 2012

T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2012

Private Selections Organic Baby Spinach, 5 oz plastic clamshell, UPC 0-11110-91128-5; Marketside Baby Spinach Organic,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Farms Retail, Inc.

FDA (openFDA food enforcement)

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Other states

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.