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.
Reported Aug 29, 2012
Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair models EMS, EMS24, HHC, and INO Powered MOV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2012
NO LABEL. Sub sandwiches are prepared fresh - made to order - wrapped in paper and then a generic label applied. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Publix Super Markets, Inc.
FDA (openFDA food enforcement)
Reported Aug 22, 2012
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Tartar Sauce sold under the following brand names: 1) Golden Corral Tartar Sauce, 1 gallon,refrigerated Product Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ken's Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Defense Nutrition Warrior Whey Natural Powder, dietary supplement, packaged in 14-oz. bottles and packed 6/14-oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Defense Nutrition
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 8, 2012
Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 8, 2012
The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Winn-Dixie Cheeseburger Macaroni Skillet Dinner WD Code 202410, Size 5.8 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winn Dixie Stores, Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2012
BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bridgepoint Medical
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Nature's Grain Garlic French Bread, 10 oz (284 g) packages,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southern Bakeries, LLC
FDA (openFDA food enforcement)
Reported Aug 1, 2012
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tripath Imaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink. GMF-RC65 Replacement Surgical Headlight Cable for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gulf Fiberoptics, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
MicroCool Breathable Impervious Surgical Gown, (Large and X-Large), Sterile, Made in Honduras. The Kimberly Clark Micro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Standard Process, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Jimmy Peppers Hot Cherry Sliced Peppers, 1 gallon plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cosmo's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Tom's Bacon Cheddar Fries, Flavored Corn and Potato Snacks, Net Wt., 2.75 oz (78.0g),
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snyder's - Lance Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.superDimension, Inc.
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.