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 48,122 notices were distributed nationwide, so they reach Alabama too — those are in the archive.

Medical devices

Reported Jul 23, 2014

ACL TOP (Base), automated coagulation laboratory instrument.

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…

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

NW Nutritional Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Vita Classic Premium Sliced Smoked Atlantic Nova Salmon, packaged in a black vacuum-sealed, plastic film package for…

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

Vita Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jul 16, 2014

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…

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

Oregon Freeze Dry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

Henora REF: 70-4026-09V1 300psi I.V. Catheter Extension Set Product Usage: Catheter extension set for high pressure…

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

RGI Medical Manufacturing, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)

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)

Medical devices

Reported Jul 9, 2014

Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.

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

Baxter Healthcare Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2014

Ocean Spray¿ Greek Yogurt Covered Craisins¿ Dried Cranberries , 8 oz Resealable Pouch UPC: #23719

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

Ocean Spray Cranberries Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 2, 2014

Dark Old Fashioned Sponge Candy, sold under the following brand and sizes: 1. Eillien's in Net Wt. 6 oz (170g) UPC…

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

Eillien's Candies, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2014

MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Ingenia 3.0T R5, magnetic resonance imaging system.

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

Philips Medical Systems, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Integra UCR 3mm Hex, Large Axial Driver. The UCR Hex Axial Driver is a surgical instrument used to implant and remove…

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

SeaSpine Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach…

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

The Anspach Effort, Inc.

44 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2014

Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

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.