All recall categories

Recalls distributed in Alabama

These notices name Alabama 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.

3,229 stored notices name Alabama, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,123 notices were distributed nationwide, so they reach Alabama too — those are in the archive.

Medical devices

Reported Dec 26, 2012

ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a…

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

ThyssenKrupp Access Corp.

FDA (openFDA device enforcement)

Food

Reported Dec 19, 2012

Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…

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

Berres Brothers, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2012

The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2012

Organic Gelato Chocolate Peanut Butter, 5 liter, contained in plastic packaging, manufactured by Fresca Foods, CO.

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

Boulder Ice Cream

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2012

Sara Lee Butter Streusel Coffee Cake, Net Wt. 11.5 oz ; 8 cakes per 5.75 lb case; Distributed by Sara Lee Corp.,…

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

Hillshire Brands Company

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2012

Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…

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

Invivo Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2012

Colby , Sizes could be 8 oz, 5lbs, 10lb, or 25lbs- vacuum packed

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

Kennys Farmhouse Cheese

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2012

Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

24 Fr 8mm Sft Flow Str Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta…

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

Terumo Cardiovascular Systems Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 5, 2012

Almondine Wedding Cookies sold by the pound.

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

Whole Foods Market South Seafood Distribution

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2012

IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention of pulmonary complications as a result of…

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

KCI USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…

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

Stryker Orthobiologics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2012

Frozen Publix Brand Premium Tempura Shrimp, 11 oz box packed 10 boxes per case.

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

Publix Corporate Office

FDA (openFDA food enforcement)

Medical devices

Reported Nov 14, 2012

Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Clinical Diagnostic Solutions

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2012

Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary rods (nails) are generally rod-shaped…

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

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2012

Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2012

The Nut Shop (brand) Roasted Peanuts, 3.0 oz MIN Wt.

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

Williams and Company Inc. dba The Nut Shop

FDA (openFDA food enforcement)

Medical devices

Reported Nov 7, 2012

HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…

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

Heartsine Technologies, Limited

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.