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 Aug 19, 2015

GE Optional Laser Centering Device X-ray generator.

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

GE Inspection Technologies, LP

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2015

Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2015

Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2015

Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes…

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

Mason Vitamins, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 12, 2015

***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120…

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

MedOp Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2015

Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 12, 2015

Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Foods Group USA LLC Cherry Hill, NJ 08003-3620 UPC…

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

Pinnacle Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2015

18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Blow bags included Product Usage: The Breath Alcohol Detector…

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

Acon Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 5, 2015

Atkins Chocolate Candies  5 ct. cartons - UPC code 637480075558

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

Atkins Indiana Distribution Center

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 5, 2015

Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…

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

Dairy Farmers OF America Inc.

33 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 5, 2015

Invivo Expression MRI Patient Monitoring System.

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP, REF 19-4137, STERILE EO, Rx only. Apply clamps parallel to the skin with the…

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

Symmetry Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.

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

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT cSystem is intended for In Vitro…

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

American Catheter / Cholangiogram Catheter 9100 Series.

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

American Catheter Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Bausch & Lomb SofPort Advanced Optics Aspheric Lens

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

Bausch & Lomb Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, Rx Only, REF…

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

Biomet Spine, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…

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

DePuy Orthopaedics, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For 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 Jul 29, 2015

0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…

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)

Medical devices

Reported Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…

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

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

Sorin Stockert Heater-Cooler 3T, 230 V Temperature control for extracorporeal perfusion of durations up to 6 hours.

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

Sorin Group USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Sysco International Whole Segments Mandarin Oranges In Light Syrup Net Wt. 6 LB 10 OZ (3.01 kg) NDC: 074865629065; 6…

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

Sysco Corporation

FDA (openFDA food 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.