State

Alabama product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47626–47650 of 80195

SevereFDA (Devices)·Z-1538-2017·2017-05-03
Heartware Recalls HVAD System Controllers for Exchange
Heartware is recalling all HVAD System Controllers currently on the market to exchange them for the next generation HVAD Controller (Controller 2.0).
Product
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System…
Category
Medical Device
Distribution
37 states
SevereFDA (Food)·F-1893-2017·2017-05-03
Pepper Colby-Jack Cheese Recalled for Potential Listeria Contamination
Deutsch Kase Haus, LLC is recalling various brands of pepper cheese due to potential Listeria monocytogenes contamination. The product was distributed across 11 states.
Product
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Walnut Creek…
Category
Food
Distribution
11 states
SevereFDA (Food)·F-2099-2017·2017-05-03
Guggisberg Cheese Recalls Butter Cheese for Potential Listeria Contamination
Guggisberg Cheese Inc is recalling Amish Creamery Butter Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.
Product
Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib Distributed by: Guggisberg Cheese, 5060 S.R. 557, Millersburg, OH 44654
Category
Food
Distribution
13 states
SevereFDA (Food)·F-2103-2017·2017-05-03
Guggisberg Garden Vegetable Natural Cheese Recalled for Listeria Risk
Guggisberg Cheese Inc is recalling Garden Vegetable Natural Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.
Product
GUGGISBERG GARDEN VEGETABLE NATURAL CHEESE INGREDIENTS: Pasterized Milk, Cultures, Red & Green Pell Peppers, Parsley, Salt, Onion, Celery, Carrots, Cucumbers, Califlower, Enzymes, LIve Yogurt Cultures 11275 W 250 N MIDDLEBURY, IN 46540
Category
Food
Distribution
13 states
SevereFDA (Drugs)·D-0686-2017·2017-05-03
Isomeric Pharmacy Recalls Testosterone Injection Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.
Product
Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V298000·2017-05-03
Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Crack Risk
Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Product
AUDI — AUDI Q5, Q7
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2101-2017·2017-05-03
Guggisberg Cheese Recalls Colby Cheese for Potential Listeria Contamination
Guggisberg Cheese Inc is recalling Colby Cheese sold under multiple brands due to potential Listeria monocytogenes contamination.
Product
Colby Cheese sold under the following brand names: Amish Classic 6lb & 15lb, Dietz & Watson 6lb, Dutch Farms 6lb, Guggisberg 8oz, 12oz, 1ib, 6lb, 14lb & 15lb, Lipari 6lb & 15lb, Meijer & Walnut Creek 6lb & 15lb
Category
Food
Distribution
13 states
SevereFDA (Drugs)·D-0685-2017·2017-05-03
Isomeric Pharmacy Recalls Injection Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 851 vials of a multi-dose injection product because production processes cannot assure sterility.
Product
Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1101, barcode 3 70285 11013 9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0681-2017·2017-05-03
Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.
Product
Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2095-2017·2017-05-03
ConAgra Recalls Premium Hunt's Chili Kits for Potential Salmonella
ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.
Product
Premium Hunt's Chili Kit, Total NET WT 44.8 OZ (2.80 LB) 1.27kg; Directions: 1) Cook and stir meat in saucepan over medium-high 7 minutes or until done; drain. 2) Stir in all remaining ingredients; simmer 10 minutes, stirring occasionally. Con Agra Foods, P.O BOX 3768, Dept.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2017·2017-05-03
Remel Blood Agar Plates Recalled for Listeria Contamination
Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.
Product
Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1877-2017·2017-05-03
Cardiovascular Systems Recalls ViperWire Advance Guide Wires Due to Packaging Error
Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.
Product
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14. Product Usage: The Stealth 360 Orbital PAD System and the Diamondback 360 Peripheral Orbital Atherectomy System are percutaneous orbital atherectomy systems…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2017·2017-05-03
Ulrich Medical Recalls uNion Cervical Plate System for Screw Mechanism Defect
Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.
Product
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0684-2017·2017-05-03
Isomeric Pharmacy Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.
Product
Triamcinolone Diacetate 40 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1021, barcode 3 70285 10211 0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1889-2017·2017-05-03
Merit Medical Recalls 1 mL Medallion Syringes Due to Plunger Tip Defect
Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.
Product
1 mL Medallion¿ Syringe. Catalog Numbers: 701989001, K01-05197P, MSS011-YP, K01-07946P, MSS011, MSS011-LB, MSS011-R, MSS011-Y, MSS011P, MSS011-LBP, MSS011-DG, K08-02926AP, K01-07742P, K10-05457P.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1884-2017·2017-05-03
XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error
XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.
Product
5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0679-2017·2017-05-03
Novartis Recalls Pilocarpine Hydrochloride Ophthalmic Solution for Impurity Failures
Novartis Pharmaceuticals Corp. is recalling Pilocarpine Hydrochloride Ophthalmic Solution 4% due to failed impurities and degradation specifications.
Product
PILOCARPINE HYDROCHLORIDE — PILOCARPINE HYDROCHLORIDE (PILOCARPINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1875-2017·2017-05-03
Siemens ACUSON S Family Ultrasound Systems Recalled for Image Display Defects
Siemens is recalling 2,045 ACUSON S Family ultrasound systems because the 18L6 HD transducer may display a triple image or a dark band, potentially affecting diagnostic accuracy.
Product
18L6 HD transducer on the ACUSON S Family ultrasound systems with software versions VD10A or VD10C; Model numbers: 18L6 HD transducer 10041227 & 10789400 S1000 10441701 S2000 10041461 S2000 (Refurb) - 10440017 S3000 10441730 Radiology: The ultrasound imaging…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2145-2017·2017-05-03
Fresh Express Organic Marketside Spring Mix Recalled for Foreign Animal Matter
Fresh Express is recalling Organic Marketside Spring Mix because foreign animal matter was allegedly found in a single container. The product was distributed in five states.
Product
Organic Marketside Spring Mix, net Wt. 5 oz. (142g) packed in rigid plastic container, UPC code 6 8113132897 5.
Category
Food
Distribution
5 states
LowFDA (Drugs)·D-0678-2017·2017-05-03
Novartis Recalls Isopto Carpine Eye Drops for Impurity Failures
Novartis Pharmaceuticals is recalling specific lots of Isopto Carpine eye drops due to failed impurities and degradation specifications.
Product
Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4%, packaged in 15 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc. Fort Worth Texas 76134 USA NDC 0998-0206-15
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1876-2017·2017-05-03
Becton Dickinson Recalls Trypticase Soy Agar and Chocolate Agar I-Plates
Becton Dickinson is recalling one lot of Trypticase Soy Agar and Chocolate Agar I-Plates because they may fail to recover specific Haemophilus organisms.
Product
BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX) I Plate Product Usage: Testing - Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastidious organisms and for the visualization of…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V292000·2017-05-02
Forest River Recalls 2014 XLR Toyhaulers Due to Axle Bolt Issue
Forest River is recalling 2014 XLR Hyperlite toyhaulers because an axle bolt may not be properly seated, which could cause the axle to shift and lead to a loss of vehicle control.
Product
FOREST RIVER — FOREST RIVER XLR
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·17144·2017-05-02
HoMedics Recalls Handheld Massagers Due to Electric Shock and Burn Hazards
HoMedics is recalling about 400,000 handheld massagers because the power cord can break and expose wires, posing electric shock and burn risks.
Product
HoMedics handheld massagers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V299000·2017-05-02
Prevost Recalls Motor Coaches Due to Trailer Hitch Fastener Loosening Risk
Prevost is recalling 2014-2017 motor coaches because trailer hitch fasteners may loosen, potentially causing the hitch to detach and increasing crash risk.
Product
PREVOST — PREVOST X3-45, H3-45, H3-45 VIP, X3-45 VIP
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V300000·2017-05-02
Prevost Recalls 2016-2017 X3-45 Vehicles for Missing Front Amber Reflectors
Prevost is recalling 2016-2017 X3-45 vehicles because they lack required front amber reflex reflectors, which may reduce side visibility and increase crash risk.
Product
PREVOST — PREVOST X3-45
Category
Vehicle
Distribution
Distributed nationwide