State

Alabama product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40676–40700 of 80184

HighFDA (Devices)·Z-2870-2018·2018-08-29
GE Healthcare Recalls CT Systems Due to Damaged Cable Electrical Hazard
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold under the following product names: CT GOLDSEAL LIGHTSPEED ULTRA, CT OPTIMA 660, CT OPTIMA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2864-2018·2018-08-29
Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Upgrades (Stitching Patient Support) 712083
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2834-2018·2018-08-29
Liebel-Flarsheim Direct Digital Imaging System Recalled for Software Display Discrepancy
Liebel-Flarsheim is recalling 28 Direct Digital Imaging Systems due to a software issue causing significant discrepancies between display and dosimeter readings in pediatric modes.
Product
Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requiring a beam of diagnostic quality radiation, primarily for urological applications such as functional x-ray diagnostics…
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-2853-2018·2018-08-29
Philips DigitalDiagnost 4.1 Chest X-Ray Unit Recalled for Footplate Hazard
Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2868-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Hook Recall
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2859-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2867-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Recall for Injury Risk
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2845-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators or patients.
Product
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2841-2018·2018-08-29
Philips DigitalDiagnost 2.x Upgrades Recalled Due to Footplate Injury Risk
Philips is recalling two DigitalDiagnost 2.x Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to operators or patients.
Product
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2872-2018·2018-08-29
GE Healthcare Optima CT540 Systems Recalled for Damaged Cable Hazard
GE Healthcare is recalling Optima CT540 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT540. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.Sold under the following product names: BEIJING CT OPTIMA 540, BEIJING OPTIMA, BEIJING OPTIMA 540, BEIJING OPTIMA 540 ASIR, CT BEIJING…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2862-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall Due to Injury Risk
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2752-2018·2018-08-29
Handicare C Series Patient Lifts Recalled for Premature Strap Wear
Handicare USA Inc. is recalling 716 C Series Patient Lifts because straps may wear and break prematurely at maximum weight conditions.
Product
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2856-2018·2018-08-29
Philips DigitalDiagnost Classic 1.x Upgrades Recalled for Footplate Safety Hazard
Philips is recalling DigitalDiagnost Classic 1.x Upgrades because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2887-2018·2018-08-29
CAREstream ProNox Nitrous Oxide Delivery Systems Recalled for High Gas Levels
CAREstream Medical LLC is recalling 919 ProNox Nitrous Oxide Delivery Systems because two units delivered higher levels of nitrous oxide than specified during routine testing.
Product
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b. CMI-0100-PNX-HS, Pro-Nox Complete Hospital Roll Stand System - Nitrous Oxide Delivery System; c. CMI-0100-PNX-HS-NO2H, Pro-Nox Hospital System…
Category
Medical Device
Distribution
47 states
HighFDA (Food)·F-1841-2018·2018-08-29
TeaSource Roasted Chestnut Loose Leaf Tea Recalled for Undeclared Almonds
TeaSource is recalling Roasted Chestnut loose leaf tea because it contains undeclared slivered almonds. The product was distributed in 17 states.
Product
TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2 oz. resealable foil bags. teasource.com, 2616 Cleveland Ave N, Roseville, MN 55113.
Category
Food
Distribution
17 states
HighFDA (Devices)·Z-2855-2018·2018-08-29
Philips DigitalDiagnost 4.1 High Performance Footplate Recall Issued
Philips is recalling DigitalDiagnost 4.1 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2852-2018·2018-08-29
Philips DigitalDiagnost 4.1 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost 4.1 units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4.1 (Stitching Patient Support) 712225
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2851-2018·2018-08-29
Philips DigitalDiagnost 4 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost 4 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2863-2018·2018-08-29
Philips DigitalDiagnost Single Detector Footplate Hook Recall
Philips is recalling DigitalDiagnost Single Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Single Detector (Stitching Patient Support) 712020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2865-2018·2018-08-29
Philips DigitalDiagnost Dual-Detector Recall for Footplate Safety Hazard
Philips is recalling DigitalDiagnost Dual-Detector units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2846-2018·2018-08-29
Philips BuckyDiagnost Ceiling System Recalled for Footplate Safety Hazard
Philips is recalling BuckyDiagnost Ceiling Systems because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
Product
BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2857-2018·2018-08-29
Philips DigitalDiagnost Classic Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Classic units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2871-2018·2018-08-29
GE Healthcare Optima CT660 Recall for Damaged Cable Electrical Hazard
GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT660. Sold under the following product names: BEIJING OPTIMA CT660 PRO GT170, BEIJING OPTIMA CT660 PRO GT200, BEIJING OPTIMA CT660S PRO 32 S, CT GOLDSEAL, CT GOLDSEAL OPTIMA 660, CT GOLDSEAL OPTIMA 660 UT-BUC, CT OPTIMA 660 LNG HN P20, CT OPTIMA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2866-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Single-Detect units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2916-2018·2018-08-29
Johnson & Johnson Recalls 1-Day ACUVUE MOIST Contact Lenses
Johnson & Johnson Vision Care is recalling specific lots of 1-Day ACUVUE MOIST contact lenses due to reports of partially formed lenses that appear smaller and stiffer.
Product
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in…
Category
Medical Device
Distribution
Distributed nationwide