State

Alabama product recalls

72,940 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,341
Critical: 1,121
Severe: 1,337
Most recent: 2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3901–3925 of 79281

HighFDA (Devices)·Z-0968-2026·2025-12-31
Femoral nails, 340 mm right trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 22 Affixus Antegrade Femoral Nails, model 815509340, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509340 Software Version: N/A Product Description: Affixus 9 mm, Length 340 mm, Right, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0974-2026·2025-12-31
Femoral nails, 300 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 11 Affixus Antegrade Femoral Nails, model 815609300, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609300 Software Version: N/A Product Description: Affixus 9 mm, Length 300 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0986-2026·2025-12-31
Campylobacter LYFO DISK controls recalled over failure to recover the organism
Microbiologics is recalling LYFO DISK units for Campylobacter jejuni because affected units may fail to recover the target microorganism.
Product
LYFO DISK, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0963-2026·2025-12-31
Cranial tracker devices recalled over an error message preventing use
Howmedica Osteonics is recalling 320 Stryker CranialMask Trackers because activating the device during surgery produces an error message that makes the device unusable.
Product
The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit for the LEDs which includes its own battery power supply. The measured LED positio
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0348-2026·2025-12-31
Sinus Cap herbal capsules recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 38 bags of Sinus Cap Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag
Category
Food
Distribution
12 states
ModerateFDA (Devices)·Z-0985-2026·2025-12-31
Campylobacter six-pack control kits recalled over failure to recover the organism
Microbiologics is recalling 18 KWIK-STIK 6-Pack units for Campylobacter jejuni because affected units may fail to recover the target microorganism.
Product
KWIK-STIK 6-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0346-2026·2025-12-31
Organic ginger root capsules recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 48 bags of Organic Ginger Root Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0341-2026·2025-12-31
Baby Allergy herbal supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 23 bottles of Baby Allergy Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0344-2026·2025-12-31
Chaga mushroom supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 144 bottles of Chaga Mushroom Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0343-2026·2025-12-31
Boswellia herbal supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 278 bottles of Boswellia Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0347-2026·2025-12-31
Pain Away herbal supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 275 bottles of Pain Away Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0345-2026·2025-12-31
Mullein ear drops recalled over unapproved drug claims and missing supplement facts
A New Life Herbs is recalling 22 bottles of Ear Drops Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0340-2026·2025-12-31
Anti-virus herbal supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 116 bottles of Anti-virus Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429
Category
Food
Distribution
12 states
ModerateFDA (Food)·H-0342-2026·2025-12-31
Baby Soothe herbal supplement recalled over unapproved drug claims and misbranding
A New Life Herbs is recalling 49 bottles of Baby Soothe Herbal Supplement over unapproved drug claims on the labeling and misbranding for having no Supplement Facts label.
Product
Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle
Category
Food
Distribution
12 states
ModerateFDA (Devices)·Z-0984-2026·2025-12-31
Campylobacter control kits recalled because they may fail to recover the organism
Microbiologics is recalling 86 KWIK-STIK 2-Pack units for Campylobacter jejuni because affected units may fail to recover the target microorganism.
Product
KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V913000·2025-12-29
Gillig Recalls 2025 Low Floor Buses Due to Loose Axle Fasteners
Gillig is recalling 2025 Low Floor transit buses because improperly tightened rear axle fasteners may cause component damage and increased crash risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0309-2026·2025-12-24
Organic moringa leaf powder recalled after contamination with Salmonella
Lexunder is recalling 701 units of Food to Live brand Organic Moringa Leaf Powder contaminated with Salmonella. The FDA has classified the action as Class I.
Product
Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2 lb., 4 lb., 8 lb., 16 lb., and 44 lb. bags; Ingredients: ORGANIC MORINGA LEAF POWDER; UPC: 8 oz - 840374833268 1 lb. - 840374812881 2 lb. - 840374813109 4 lb. -
Category
Food
Distribution
38 states
CriticalFDA (Devices)·Z-0914-2026·2025-12-24
Carestation 750 anesthesia systems recalled over potential unexpected shutdown
GE Medical Systems is recalling 888 Carestation 750 series anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The action is Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000; Products for which affected PMB can be used as a spare part: Carestatio
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0913-2026·2025-12-24
Anesthesia systems recalled over potential unexpected shutdown on mains power loss
GE Medical Systems is recalling 1,277 Carestation anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The FDA has classified the action as Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF 1012-9620
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0310-2026·2025-12-24
Organic supergreens powder mix recalled after contamination with Salmonella
Lexunder is recalling 159 units of Food to Live brand Organic Supergreens Powder Mix contaminated with Salmonella. The FDA has classified the action as Class I.
Product
Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 1.5 lb., 3 lb., 6 lb., 12 lb.; Ingredients: ORGANIC KALE; ORGANIC MORINGA LEAF; ORGANIC WHEAT GRASS; ORGANIC SPIRULINA UPC: 8 oz. - 810097461475 1 lb. - 8100974
Category
Food
Distribution
38 states
CriticalFDA (Devices)·Z-0915-2026·2025-12-24
Anesthesia power management boards recalled over potential unexpected system shutdown
GE Medical Systems is recalling 203 Carestation anesthesia system Power Management Board field replaceable units over potential unexpected shutdown if AC mains power is lost.
Product
GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0961-2026·2025-12-24
Chemistry analyzer control modules recalled over software that may give erroneous results
Abbott Laboratories is recalling 11,653 Alinity ci-series System Control Modules because software versions 3.6.1 and lower could lead to erroneous results for multiple analytes.
Product
Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0921-2026·2025-12-24
Sterile operating room scissors recalled over weak seals affecting sterility
Medline is recalling 56 sterile operating room scissors because weak packaging seals may result in a breach of sterility and an increased risk of infection if the product is used.
Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0941-2026·2025-12-24
Imaging viewer software recalled over inaccurate length measurement values
DICOM Grid is recalling 924 units of Intelerad InteleShare software because a bug can produce inaccurate length measurement tool values that could lead to misdiagnosis.
Product
Intelerad InteleShare software, with ProViewer component
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0922-2026·2025-12-24
Sterile Kelly forceps recalled over weak seals that may breach sterility
Medline is recalling 53 sterile Kelly forceps because weak packaging seals may result in a breach of sterility and an increased risk of infection if the product is used.
Product
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
Category
Medical Device
Distribution
Distributed nationwide