The Recall Desk

State

Alabama product recalls

73,741 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,377
Critical
1,129
Severe
1,604
Most recent
2026-10-28

Of the 6,377 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 1,604 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36226–36250 of 80118

  • SevereFDA (Drugs)·D-1328-2019·2019-06-19

    Pharm D Solutions Recalls Lipo MIC-12 Injectable Vials for Sterility Concerns

    Pharm D Solutions, LLC is recalling 669 vials of Lipo MIC-12 injectable solution due to a lack of sterility assurance. The product was distributed nationwide.

    Product
    Lipo MIC-12 (Methylcobalamin, USP 1mg, Methionine USP 15mg, Inositol, FCC 50mg, Choline Chloride, FCC 100 mg) 10 mL Injectable vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1330-2019·2019-06-19

    Pharm D Solutions Recalls Sermorelin/Ipamorelin Vials Due to Sterility Concerns

    Pharm D Solutions is recalling Sermorelin/Ipamorelin 18 mg/15 mg vials because they lack sterility assurance. The recall covers 24 vials distributed nationwide.

    Product
    Sermorelin/Ipamorelin 18 mg/15 mg, 10mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1325-2019·2019-06-19

    Pharm D Solutions Recalls Human Chorionic Gonadotropin Vials for Sterility Concerns

    Pharm D Solutions is recalling 279 vials of Human Chorionic Gonadotropin 5,000 IU due to a lack of sterility assurance. The recall covers products distributed nationwide.

    Product
    Human Chorionic Gonadotropin 5,000 IU vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1405-2019·2019-06-19

    Synthetopes Recalls Sn-Tetrofosmin Kits Due to Processing Control Deficiencies

    Synthetopes Inc is recalling Sn-Tetrofosmin Kits nationwide due to a lack of processing controls. All lots remaining within their expiry date are affected.

    Product
    Sn-Tetrofosmin Kit 5.0 mL, Thaw and Vent before use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1326-2019·2019-06-19

    Pharm D Solutions Recalls Human Chorionic Gonadotropin Vials for Sterility Concerns

    Pharm D Solutions is recalling 104 vials of Human Chorionic Gonadotropin 12,000 IU due to a lack of sterility assurance.

    Product
    Human Chorionic Gonadotropin 12,000 IU vials Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1332-2019·2019-06-19

    Pharm D Solutions Recalls Sermorelin/GHRP-2 Vials Due to Sterility Concerns

    Pharm D Solutions is recalling 66 vials of Sermorelin/GHRP-2 because they lack sterility assurance. The products were distributed nationwide.

    Product
    Sermorelin/GHRP-2 9 mg/6 mg vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V472000·2019-06-19

    BMW Recalls 2008-2012 Models for Battery Cable Defect

    BMW is recalling specific 2008-2012 models because a battery cable connection may degrade, causing power loss and stalling.

    Product
    BMW — BMW M3, 328I, 328XI, 335D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1327-2019·2019-06-19

    FDA Recalls Ipamorelin Acetate Injectable Vials Due to Sterility Concerns

    Pharm D Solutions is recalling 11 vials of Ipamorelin Acetate 9 mg/9mL Injectable due to a lack of sterility assurance.

    Product
    Ipamorelin Acetate 9 mg/9mL Injectable vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1323-2019·2019-06-19

    Pharm D Solutions Recalls B-Complex Injectable Vials Due to Sterility Concerns

    Pharm D Solutions, LLC is recalling specific lots of B-complex injectable vials due to a lack of sterility assurance. The affected product is distributed nationwide.

    Product
    B-complex (Thiamine 100mg, Riboflavin 2mg, Niacinamide 100 mg, Pyridoxine 2mg, Depanthenol 5mg) injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846, NDC 69699-1611-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1752-2019·2019-06-19

    GE Healthcare Recalls Proteus XR/a Radiographic Systems Due to Monitor Fall Risk

    GE Healthcare is recalling 825 Proteus XR/a radiographic systems because a monitor fell off its wall mount due to product aging.

    Product
    Proteus XR/a The Proteus XR/a radiographic system offers the flexibility to choose a configuration based upon your specific requirements. The system provides exceptional image quality, high frequency X-ray generation, easy patient positioning, intuitive operator control and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1755-2019·2019-06-19

    GE Healthcare Recalls Silhouette VR Systems Due to Monitor Mount Failure

    GE Healthcare is recalling 825 Silhouette VR systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-saving design.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1775-2019·2019-06-19

    Conformis iTotal Hip Replacement System Recalled for Dimensional Discrepancy

    Conformis, Inc. is recalling 128 iTotal Hip Replacement System stems due to a 3mm discrepancy between approved and manufactured neck/head lengths.

    Product
    Conformis iTotal Hip Replacement System: HBS-033-00xx-010101, (HIP-PATIENT SPECIFIC STEM LEFT)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1779-2019·2019-06-19

    Skytron Integrity 270 Steam Sterilizer Recalled for Weld Fatigue

    Skytron is recalling five Integrity 270 Steam Sterilizers because the weld attaching the air heater assembly has shown signs of fatigue or failure.

    Product
    Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1447-2019·2019-06-19

    Izzio Artisan Bakery 100% Rye Bread Recalled for Undeclared Wheat

    Izzio Artisan Bakery is recalling 100% Rye Bread because it may contain undeclared wheat. The product was distributed nationwide.

    Product
    Izzio Artisan Bakery 100% Rye Bread, Net Weight: 9 oz ; 8 slices per package, Flow Wrap Package. Frozen. Item #3301, Case UPC #657082033015, Unit UPC #657082033015
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V473000·2019-06-19

    Audi Recalls 2019 Q5 and SQ5 Models for Air Bag Defect

    Volkswagen Group of America is recalling 2019 Audi Q5 and SQ5 vehicles because a defective instrument panel carrier may damage the passenger air bag during a crash.

    Product
    AUDI — AUDI Q5, SQ5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1753-2019·2019-06-19

    GE Healthcare Recalls Prestilix 1600X Digital Radiology Systems

    GE Healthcare is recalling 825 Prestilix 1600X digital radiology systems because a monitor fell off its wall mount due to product aging.

    Product
    Prestilix 1600X Prestilix system is a fully integrated remote controlled digital radiology system. It is designed for all general radiology applications with or without contract injection and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2019·2019-06-19

    Medtronic InterStim System Recall for Unexpected Stimulation Increase

    Medtronic is recalling InterStim System kits due to a potential for unexpected stimulation increases during programming with the A10 Clinician Application.

    Product
    InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1778-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling 40 Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1777-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling four Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2019·2019-06-19

    Terumo Electronic Patient Gas System Recalled for Control Slider Failure

    Terumo is recalling 72 Electronic Patient Gas Systems used in cardio-pulmonary bypass because a fault disables control sliders, forcing use of local knobs.

    Product
    Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI 00886799000588. Used in cardio-pulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E041000·2019-06-19

    Gillig Recalls Transpec T287X Series Glass Roof Hatches for Shattering Risk

    Gillig LLC is recalling Transpec T287X Series glass roof hatches sold as aftermarket parts because temperature and vibration stresses may cause the tempered glass to shatter, potentially injuring passengers.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V474000·2019-06-19

    Audi Recalls Vehicles Due to Passenger Air Bag Deactivation Risk

    Audi is recalling specific 2015-2019 models because an electrical issue may cause the passenger air bag to deactivate, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET, RS 3, A3 SPORTBACK E-TRON, S3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1399-2019·2019-06-19

    Synthetopes Recalls Pentreotide Vials Due to Lack of Processing Controls

    Synthetopes Inc. is recalling Pentreotide (10 uGm) vials nationwide due to a lack of processing controls. All lots remaining within expiry are affected.

    Product
    Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1342-2019·2019-06-19

    Chiesi Recalls Zileuton Extended-Release Tablets Due to Dissolution Failure

    Chiesi USA is recalling 2,598 bottles of Zileuton Extended-Release Tablets, 600 mg, because they failed dissolution specifications.

    Product
    Zileuton Extended-Release Tablets, 600 mg, 120-count bottles, Rx only, Distributed by: Prasco Laboratories, Mason, OH 45040 USA; NDC 66993-485-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1751-2019·2019-06-19

    GE Healthcare Recalls Prestige Systems Due to Monitor Mount Failure

    GE Healthcare is recalling Prestige II, SI, and VH systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.
    Category
    Medical Device
    Distribution
    Distributed nationwide