State

Alabama product recalls

73,833 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,378
Critical: 1,129
Severe: 1,605
Most recent: 2026-11-04

Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52851–52875 of 80211

CriticalFDA (Drugs)·D-0970-2016·2016-06-15
FDA Recalls Asia Black 25 Ephedra Extreme Fat Burner for Unapproved Ingredients
Novacare, LLC is recalling Asia Black 25 Ephedra Extreme Fat Burner because FDA sampling confirmed the presence of salicylic acid, an unapproved ingredient in dietary supplements.
Product
Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0960-2016·2016-06-15
Fuel Up High Octane capsules recalled for undeclared sildenafil analogue
Reesna, Inc. is recalling Fuel Up High Octane capsules because they contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug Sildenafil.
Product
FUEL UP HIGH OCTANE, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0957-2016·2016-06-15
Baxter Recalls Sodium Chloride Injection Due to Insect Particulate Matter
Baxter Healthcare is recalling 255,852 bags of 0.9% Sodium Chloride Injection because customers reported finding an insect in the primary container.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0962-2016·2016-06-15
FDA Recalls Thermo FX Supplement for Unapproved Salicylic Acid
Novacare, LLC is recalling The People's Chemist Thermo FX Barely Legal Thermogenic Aid because FDA sampling confirmed the presence of salicylic acid in the product.
Product
The People's Chemist Thermo FX Barely Legal Thermogenic Aid, packaged in 90 capsule containers. Manufactured by TPC, LLC, www.thepeopleschemist.com.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0959-2016·2016-06-15
Fuel Up Plus capsules recalled for undeclared sildenafil analogue
Reesna, Inc. is recalling Fuel Up Plus capsules marketed as a dietary supplement because they contain undeclared hydroxythiohomosildenafil, an analogue of the ED drug sildenafil.
Product
FUEL UP PLUS, capsules, a) 1-count package, b) 5-count bottle, c) 10-count bottle WWW.FUELUPPILLS.COM
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0965-2016·2016-06-15
FDA Recalls Thin and Slim Burn Fat Now Supplement for Unapproved Ingredient
Novacare, LLC is recalling Thin and Slim Burn Fat Now dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.
Product
Thin and Slim Burn Fat Now Dietary Supplement packaged in 90 capsule containers. http://www.secretsofherbs.com. Made in the USA.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0958-2016·2016-06-15
Baxter Recalls Dextrose Injection Due to Insect Contamination
Baxter Healthcare is recalling Dextrose Injection, USP, 70% due to confirmed reports of an insect found in the primary container.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0963-2016·2016-06-15
FDA Recalls MaxOut Body Fat Burner for Unapproved Salicylic Acid
Novacare, LLC is recalling MaxOut Body Fat Burner with Ephedra because FDA sampling confirmed the presence of salicylic acid in the dietary supplement.
Product
Thin and Slim MaxOut Body Max Out FX Fat Burner with Ephedra packaged in containers of 60 capsules. Distributed by Teamtrade, Inc., Ft. Lauderdale, FL. 1-866-MaxOut www.MaxOutBODY.com.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V440000·2016-06-15
Mercedes-Benz Recalls 2016 GLE450 Vehicles Due to Engine Shutdown Risk
Mercedes-Benz is recalling 5,826 model year 2016 GLE450 vehicles because a software error may cause the engine to shut down while braking, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLE450
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1426-2016·2016-06-15
Lee Seed Company Recalls Yogurt Super Soynuts for Undeclared Milk
Lee Seed Company is recalling Yogurt Super Soynuts because the product contains undeclared milk, posing a risk to individuals with milk allergies.
Product
Yogurt Super Soynuts packaged in 16 oz. plastic bags and packaged in holiday tins. Lee Seed Company, Inc., Inwood, Iowa.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0968-2016·2016-06-15
Dietary Supplement Recalled for Unapproved Salicylic Acid Content
Novacare, LLC is recalling Thin and Slim Naturally AM dietary supplements because FDA sampling confirmed the presence of unapproved salicylic acid.
Product
Thin and Slim Naturally The Natural Alternative AM Dietary Supplement packaged in 90 capsule containers. Distributed by TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0967-2016·2016-06-15
Novacare Recalls Unapproved TruTrim Supplements Containing Salicylic Acid
Novacare, LLC is recalling TruTrim dietary supplements marketed without FDA approval because they contain salicylic acid.
Product
TruTrim (product not labeled)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V437000·2016-06-15
Thor Motor Coach Tuscany Recalled for Brake Signal Defect
Thor Motor Coach is recalling 2014-2016 Tuscany motor homes because the brake signal to towed devices may not deactivate, causing dragging brakes and fire risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH TUSCANY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1927-2016·2016-06-15
GE Healthcare Recalls MSK 1.5T Extreme MR Scanners Due to Gas Venting Defect
GE Healthcare is recalling 97 MSK 1.5T Extreme MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
Product
MSK 1.5T Extreme MR Scanner, a diagnostic imaging device
Category
Medical Device
Distribution
25 states
SevereFDA (Food)·F-1425-2016·2016-06-15
Mountain Thins Trail Mix Recalled for Listeria Contamination Risk
Brown & Haley Inc. is recalling Mountain Thins Trail Mix flavor due to potential Listeria monocytogenes contamination.
Product
Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770 33370 7
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1916-2016·2016-06-15
Hill-Rom Recalls Liko Universal SlingBars Due to Center Bolt Failure Risk
Hill-Rom is recalling Liko Universal SlingBars because the center bolt may weaken and break, posing a risk of patient falls and injury.
Product
Liko Universal SlingBars Universal SlingBar" 350, Universal SlingBar" 350 QRH, Universal SlingBar" 350 R2R, Universal SlingBar" 450, Universal SlingBar" 450 QRH, Universal SlingBar" 450 R2R, Universal SlingBar" 600 Universal SlingBar" 600 QRH Component of…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0971-2016·2016-06-15
FDA Recalls Black Widow 25 Ephedra Fat Burner for Unapproved Ingredient
Novacare, LLC is recalling Black Widow 25 Ephedra Super Potent Fat Burner because FDA sampling confirmed the presence of salicylic acid in the product.
Product
Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0972-2016·2016-06-15
Methyldrene Original 25 Ephedra ECA Stack Recalled for Unapproved Salicylic Acid
Novacare, LLC is recalling Methyldrene Original 25 Ephedra ECA Stack dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug.
Product
Methyldrene Original 25 Ephedra ECA Stack Extra-Potent Fat Burner Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0961-2016·2016-06-15
FDA Recalls Fataway Ultimate Stack Supplement for Unapproved Salicylic Acid
Novacare, LLC is recalling Thin and Slim Fataway Ultimate Stack with Chromium because FDA sampling found unapproved salicylic acid in the dietary supplement.
Product
Thin and Slim Fataway Ultimate Stack with Chromium, packaged per 120 capsules. Distributed by Dale H Enterprises Inc. Lewisburg, PA 17837, www.fataway.org.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0969-2016·2016-06-15
Novacare Recalls Thin and Slim Extreme Stack Fat Burner Supplement
Novacare, LLC is recalling Thin and Slim Extreme Stack Fat Burner dietary supplements because FDA sampling confirmed the presence of salicylic acid.
Product
Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged in 90 capsule containers. TSN Labs Inc., P.O. Box 38, Midvale, UT 84047, 1-800-769-7290, www.tsn2000.com
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0973-2016·2016-06-15
Novacare Recalls Unapproved Dietary Supplements Containing Salicylic Acid
Novacare, LLC is recalling Xcellerator dietary supplements because FDA sampling confirmed the presence of salicylic acid in products marketed without an approved NDA/ANDA.
Product
Xcellerator (product not labeled)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1928-2016·2016-06-15
GE Healthcare Recalls Optima 1.5T MR430s MR Scanners Due to Gas Venting Defect
GE Healthcare is recalling 101 Optima 1.5T MR430s MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
Product
Optima 1.5T MR430s MR Scanner, a diagnostic imaging device
Category
Medical Device
Distribution
25 states
SevereFDA (Food)·F-1427-2016·2016-06-15
Publix Cranberry Nut & Seed Mix Recalled for Listeria Risk
Publix Super Markets is recalling Cranberry Nut & Seed Mix due to possible Listeria monocytogenes contamination. The product was distributed in six southeastern states.
Product
Publix Cranberry Nut & Seed Mix, 7.05 ounce plastic container. Manufactured by Publix Supermarkets in Lakeland, FL.
Category
Food
Distribution
6 states
HighFDA (Food)·F-1438-2016·2016-06-15
Frontier Co-op Hojicha Tea Recalled Due to Potential Salmonella Contamination
Frontier Natural Products CO-OP is recalling specific lots of Hojicha Tea due to potential Salmonella contamination. Consumers should stop using the affected products.
Product
16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Organic Camellia sinensus, Norway, IA 52318
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1922-2016·2016-06-15
Baxter Recalls Actifuse Bone Void Fillers Due to Endotoxin Concerns
Baxter Healthcare is voluntarily recalling Actifuse ABX and MIS System bone void fillers because they may contain endotoxin levels above specification criteria.
Product
Actifuse ABX/Actifuse MIS System A bone void filler intended only for orthopedic applications as a filler for gaps and voids that are not intrinsic to the stability of the bony structure.
Category
Medical Device
Distribution
Distributed nationwide