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.
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Ultraslim. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Photonic Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResultNet is a stand-alone software package…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc./d.b.a.Basic American Metal Products
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2014
Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2014
PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2014
ORGANIC TRADITIONS SPROUTED CHIA SEED POWDER NET WT. 8 oz. and 16 oz., UPC 854260006162, item number AHM616 and UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Health Matters America Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 3, 2014
McCormick Ground Oregano in 0.75 oz plastic bottle. UPC NUMBER: 52100003566 (as seen on label: 0-523561-6) MCCORMICK…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 3, 2014
Verigene CYP2C19 Nucleic Acid Test (CYP2C19 Test). Each CYP2C19 kit consists of 20 Verigene CYP2C19 Nucleic Acid Test…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nanosphere, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
American Spoon Food Sour Cherry Marmalade, 9.5 oz in glass jars with metal lid e. Total package size (e.g. 12 packages…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Spoon Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAMER NON-STERILE, BIOMET…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic images of the skull,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Gyrus ACMI Falope-Ring Dilator, item 000878-4. The Falope-Ring Dilator is a conical plastic device that is a component…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
CAP Change Kit w/MicroClave Clear, Item No. B78109 BD prefilled syringes are co-packaged into a kit with ICU devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Product is in a 160 gram, light green tin container, labeled in part: "ecoato Sweet Paprika Powder Product of Spain"
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
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.