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.

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.

35676–35700 of 80118

  • HighFDA (Devices)·Z-2011-2019·2019-07-31

    Philips BrightView XCT Medical Device Recalled for Handcontroller Motion Defect

    Philips Medical Systems is recalling 427 BrightView XCT devices because a handcontroller issue may cause uncommanded motions or continued motion after buttons are released.

    Product
    BrightView XCT , Model Number 882482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2026-2019·2019-07-31

    Siemens AXIOM Artis TC X-ray Generator Recall for Power Supply Issue

    Siemens is recalling one AXIOM Artis TC unit due to a power supply tolerance issue that may cause X-ray generation failure during procedures.

    Product
    AXIOM Artis TC, Model Number 7728350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2080-2019·2019-07-31

    Bard Nautilus Delta Port Kits Recalled for ECG Signal Loss

    Bard Peripheral Vascular is recalling specific Nautilus Delta Port Kits due to a risk of losing the intravascular ECG signal during placement procedures.

    Product
    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2039-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2019·2019-07-31

    Siemens AXIOM Artis dFC X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 19 AXIOM Artis dFC units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.

    Product
    AXIOM Artis dFC, Model Number 7727717
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E052000·2019-07-31

    Vitro Recalls Aftermarket Rear Window Glass for Non-Compliant Fragment Size

    Vitro is recalling 47,366 aftermarket rear window glass units for various vehicles because improper tempering may result in large fragments that increase injury risk in a crash.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2035-2019·2019-07-31

    Spacelabs Smart Disclosure System Recalled for Patient Data Mismatch

    Spacelabs Healthcare is recalling the Smart Disclosure System because patient records were printed with waveforms from other patients.

    Product
    Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E053000·2019-07-31

    Mekra Lang Recalls Truck Mirror Housings Due to Detaching Glass Risk

    Mekra Lang is recalling certain Main Mirror Housings for truck cabs because improper adhesive bonding may cause the mirror glass to detach, reducing driver visibility.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1605-2019·2019-07-31

    Flowers Foods Recalls Hot Dog Buns Due to Potential Plastic Contamination

    Flowers Foods is recalling 46,122 packages of hot dog buns sold under multiple brands because they may contain small pieces of hard plastic.

    Product
    Hot Dog Buns sold under the brand names of: CLOVER VALLEY 8CT UPC 70210 00760 1; FAMILY STYLE 8CT UPC 70210 01297 1; FLOWERS RESTAURANT 12CT UPC 70210 00640 6, UPC 70210 00649 9 & UPC 70210 00964 3; FOOD DEPOT 8CT UPC 72250 02439 6; GREAT VALUE 8CT UPC 78742 09728 2; IDEAL 8CT…
    Category
    Food
    Distribution
    18 states
  • HighNHTSA·19V564000·2019-07-31

    Hino Recalls 2020 NJ8J, NE8J, and NV8J Trucks for Mirror Glass Defect

    Hino is recalling 1,531 model-year 2020 NJ8J, NE8J, and NV8J trucks because exterior mirror glass may detach, reducing driver visibility and increasing crash risk.

    Product
    HINO — HINO NJ8J, NE8J, NV8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2042-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Concerns

    Cardinal Health is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Concerns

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1996-2019·2019-07-31

    Stanley Healthcare Recalls Arial 54315 Network Manager Due to Outages

    Stanley Healthcare is recalling 137 Arial 54315 Network Managers because they caused outages in the Arial nurse call system.

    Product
    STANLEY Healthcare Arial 54315 Network Manager
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1599-2019·2019-07-31

    Flowers Foods Recalls Dinner Rolls Due to Potential Plastic Contamination

    Flowers Foods is recalling Laura Lynn and Wonder dinner rolls because they may contain small pieces of hard plastic introduced during production.

    Product
    Dinner Rolls sold under the brand names of Laura Lynn UPC 86854 06669 0 & Wonder 12 CT UPC 72250 07421 6 24 CT UPC 72250 01169 3
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-2009-2019·2019-07-31

    Philips BrightView SPECT Recalled for Uncommanded Handcontroller Motion

    Philips Medical Systems is recalling 696 BrightView SPECT units because the handcontroller may move spontaneously or continue moving after buttons are released.

    Product
    BrightView SPECT, Model Number 882480
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2022-2019·2019-07-31

    Siemens AXIOM Artis dBA X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 85 AXIOM Artis dBA units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.

    Product
    AXIOM Artis dBA, Model Number 7555357
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2038-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health 200, LLC is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2050-2019·2019-07-31

    Cardinal Health Recalls Monoject Blunt Cannula Due to Sterility Barrier Defect

    Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas due to a manufacturing defect that could compromise the product's sterility barrier.

    Product
    Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1514-2019·2019-07-31

    Baxter Recalls Sodium Chloride Injection Due to Sterility Concerns

    Baxter Healthcare is recalling 139,680 containers of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for bags to leak.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1581-2019·2019-07-31

    Lupin Recalls Lisinopril and Hydrochlorothiazide Tablets Due to Foreign Object

    Lupin Pharmaceuticals is recalling 11,832 bottles of Lisinopril and Hydrochlorothiazide tablets because a foreign tablet was found in the product.

    Product
    LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide