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 48,100 notices were distributed nationwide, so they reach Alabama too — those are in the archive.

Medical devices

Reported Oct 24, 2018

GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:…

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

OriGen Biomedical, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - 888849000494 12 ct. Box UPC # - 888849000500

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

Quest Nutrition, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures

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

Zimmer Biomet, Inc.

47 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…

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

Bayer Medical Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Colpo-Pneumo Occluder, Part CPO-6

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…

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

Neomed Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…

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

Sarap Asian Fusion

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 10, 2018

ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…

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

Endologix

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 10, 2018

ICU Medical 14" (36 cm) Appx 3.6 ml, Bifuse Transfer Set w/Rotating Luer, REF: 14237-28 The Intravascular…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 10, 2018

Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…

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

Neighbors LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 10, 2018

TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product…

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

Varian Medical Systems

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 10, 2018

EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…

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

Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.

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

Bausch & Lomb Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

ESSENTIO Pacemaker

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

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 3, 2018

Shelled eggs in blank cardboard cases at 2.5 dozen a case. Shelled eggs in dozen cartons labeled as "Gravel Ridge Farms…

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

Gravel Ridge Farms

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…

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

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

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

Philips Electronics North America Corporation

26 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…

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

Intuitive Surgical, Inc.

1 more product in this recall

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.