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.

35526–35550 of 80118

ModerateFDA (Devices)·Z-2197-2019·2019-08-14
Siemens Lantis Commander Radiation Therapy Software Recalled for RDP Vulnerability
Siemens Medical Solutions is recalling 15 Lantis Commander units due to a Microsoft Windows Remote Desktop Protocol vulnerability.
Product
Lantis Commander, Model # 4503178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient…
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-2217-2019·2019-08-14
MedComp Recalls Hemodialysis Catheter Kits Due to Labeling Error
Medical Components, Inc. is recalling 6,830 hemodialysis catheter insertion kits because the tray labels incorrectly identify the included introducer as valved.
Product
14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2174-2019·2019-08-14
Ortho VITROS 250 Chemistry System Recalled for Software Calibration Anomaly
Ortho Clinical Diagnostics is recalling 30 VITROS 250 Chemistry Systems due to a software anomaly that may cause unsuccessful calibrations.
Product
VITROS 250 Chemistry System, clinical chemistry analyzer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1610-2019·2019-08-14
Herbal Doctor Remedies Recalls Migraine Off Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Migraine Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Migraine Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1592-2019·2019-08-14
Herbal Doctor Remedies Recalls Cardia Forte Capsules for CGMP Deviations
Herbal Doctor Remedies is recalling Cardia Forte 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Product
Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1626-2019·2019-08-14
Herbal Doctor Remedies Recalls Appetrol Capsules for CGMP Deviations
Herbal Doctor Remedies is recalling Appetrol Capsules because they were manufactured outside of current Good Manufacturing Practice controls.
Product
Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2146-2019·2019-08-14
Geistlich Bio-Oss Pen Recalled Due to Visible Plastic Debris
Geistlich Pharma is recalling Bio-Oss Pen units because visible green plastic debris was found on the outer barrel when unscrewing the cap.
Product
Geistlich Bio-Oss Pen, Sterile cancellous granules in an applicator, 0.25-1.mm 0.5g, For single use only, Part Number 20116 - Product Usage: Augmentation or reconstructive treatment of the alveolar ridge; Filling of infrabony periodontal defects; Filling of defects after root…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1620-2019·2019-08-14
Herbal Doctor Remedies Recalls Worm Off Capsules Due to Manufacturing Deviations
Herbal Doctor Remedies is recalling Worm Off 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2170-2019·2019-08-14
Centurion Driveline Management System 1 Daily Kit Recalled for Packaging Risk
Centurion Medical Products is recalling 6,180 Driveline Management System 1 Daily Kits because sterile packaging may be compromised.
Product
DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2147-2019·2019-08-14
Geistlich Bio-Oss Pen Recalled Due to Visible Plastic Debris
Geistlich Pharma North America is recalling Bio-Oss Pen applicators because a visible piece of green plastic was found on the outer barrel when unscrewing the cap.
Product
Geistlich Bio-Oss Pen, Sterile cancellous granules in an applicator, 1-2mm 0.5g, For single use only, Part Number 20126 - Product Usage: Augmentation or reconstructive treatment of the alveolar ridge; Filling of infrabony periodontal defects; Filling of defects after root…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1590-2019·2019-08-14
Herbal Doctor Remedies Recalls Baby Saver Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Baby Saver Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Baby Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1607-2019·2019-08-14
Herbal Doctor Remedies Recalls Lung Fixer Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Lung Fixer Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Lung Fixer Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2186-2019·2019-08-14
Philips Ingenuity CT Recalled for Potential Cardiac Image Labeling Error
Philips is recalling 92 Ingenuity CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.
Product
Ingenuity CT, Model # 728326, computed tomography x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1617-2019·2019-08-14
Herbal Doctor Remedies Recalls Stone Purger Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Stone Purger Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Stone Purger Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1618-2019·2019-08-14
Herbal Doctor Remedies Recalls Thyro-H Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Thyro-H 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Product
Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2182-2019·2019-08-14
Ortho VITROS 4600 Chemistry System Recalled for Software Calibration Anomaly
Ortho Clinical Diagnostics is recalling nine VITROS 4600 Chemistry Systems due to a software anomaly that may cause unsuccessful calibration.
Product
VITROS 4600 Chemistry System, clinical chemistry analyzer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2144-2019·2019-08-14
Biomet 3i Recalls Titanium Abutments Due to Manufacturing Defect
Biomet 3i is recalling 49 units of Certain Bellatek Titanium Abutments because a manufacturing defect prevents the screw from seating correctly.
Product
CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number ILDAT3 - Product Usage:BIOMET3i Restorative products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1619-2019·2019-08-14
Herbal Doctor Remedies Recalls Vertigo Off Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Vertigo Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Product
Vertigo Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1603-2019·2019-08-14
Herbal Doctor Remedies Recalls Herpes-V Balm for Manufacturing Violations
Herbal Doctor Remedies is recalling Herpes-V Balm because it was manufactured outside of required Good Manufacturing Practices controls.
Product
Herpes-V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2190-2019·2019-08-14
Philips iCT SP Computed Tomography Systems Recalled for Image Labeling Error
Philips is recalling 27 iCT SP computed tomography systems because images may be incorrectly labeled as having phase tolerance applied when it was not.
Product
iCT SP Model # 728311, computed tomography x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1601-2019·2019-08-14
Herbal Doctor Remedies Recalls Herpes-P Capsules for Manufacturing Deviations
Herbal Doctor Remedies is recalling Herpes-P 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Product
Herpes-P, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2184-2019·2019-08-14
Ortho VITROS 5,1 FS Chemistry System Recalled for Software Calibration Issue
Ortho Clinical Diagnostics is recalling 55 VITROS 5,1 FS Chemistry Systems due to a software anomaly that may cause unsuccessful calibrations.
Product
VITROS 5,1 FS Chemistry System, clinical chemistry analyzer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2100-2019·2019-08-14
ASTRA Lidar System Recalled for Incorrect Class 1 Laser Labeling
ASTRA, LLC is recalling one Lidar System for Erosion Flume Application due to incorrect labeling of a Class 1 laser product.
Product
Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1595-2019·2019-08-14
Dragon Pain Oil Recalled for Manufacturing Process Deviations
Herbal Doctor Remedies is recalling Dragon Pain Oil because it was manufactured outside of required Good Manufacturing Practices controls.
Product
Dragon Pain Oil, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2159-2019·2019-08-14
DRG Salivary Testosterone ELISA Recalled for Inaccurate Low-Range Results
DRG Instruments GmbH is recalling 38 kits of Salivary Testosterone ELISA because the assay may report testosterone levels that are too low.
Product
DRG Salivary Testosterone ELISA- IVD for the detection of Testerone in human saliva Catalog # SLV-3013 Product Usage: The Salivary Testosterone ELISA (SlV-3013) is an enzymatic in vitro Assay for the detection of Testosterone in human Saliva. Testosterone levels are…
Category
Medical Device
Distribution
Distributed nationwide