State

Alabama product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30651–30675 of 80099

SevereFDA (Devices)·Z-2476-2020·2020-07-15
Verathon Recalls GlideScope Core OneTouch Smart Cables Due to Connection Defect
Verathon is recalling 437 GlideScope Core OneTouch Smart Cables because twisting during connection may damage the internal circuit board, causing video loss during critical intubation procedures.
Product
GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch Cables (Reusable Device) is ancillary equipment used with the Core 10 and Core 15 monitors. The monitor and workstation are intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2528-2020·2020-07-15
TeDan Phantom CS Quick Start Distraction Screw Recall for Seal Defect
TeDan Surgical Innovations LLC is recalling 730 sterile Phantom CS Quick Start Distraction Screws due to a lack of pouch seal.
Product
PHANTOM CS QUICK START DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2497-2020·2020-07-15
Ra Medical Systems Recalls DABRA Laser Due to Software Issue
Ra Medical Systems is recalling 79 DABRA Laser units because a software issue could cause unintended laser light release, potentially injuring users or patients.
Product
DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA Laser System". The system is designed to deliver the energy to the surgical site to ablate unwanted material. The…
Category
Medical Device
Distribution
22 states
HighCPSC·20148·2020-07-15
Simplers Botanicals Wintergreen Essential Oil Recalled for Packaging Defect
Nutraceutical is recalling Simplers Botanicals Wintergreen Essential Oil because the packaging is not child-resistant, posing a poisoning risk.
Product
Simplers Botanicals Organic Wintergreen (Gaultheria Fragrantissiam) Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20149·2020-07-15
Crate and Barrel Recalls Parke Twin and Full Beds Due to Fall Hazard
Crate and Barrel is recalling Parke twin and full beds because the headboard can separate from the frame, posing a fall hazard.
Product
Parke Twin and Full Beds
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2492-2020·2020-07-15
Prodimed Combicath Paediatric Catheters Recalled for Sterility Assurance Issues
Prodimed is recalling Combicath Paediatric catheters due to a lack of assurance of sterility. The recall covers 2,580 units distributed nationwide.
Product
Prodimed Combicath Paediatric catheters for blind protected distal bronchial sampling-" COMBICATH PE 35 cm Product Code: 58 223 19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2529-2020·2020-07-15
TeDan Phantom CS Distraction Screw Recalled for Sterility Seal Defect
TeDan Surgical Innovations LLC is recalling 495 Phantom CS Quick Start Distraction Screws because the pouch seal is lacking, compromising the sterile labeling.
Product
PHANTOM CS QUICK START DISTRACTION SCREW, 14 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2487-2020·2020-07-15
Prodimed Combicath Catheters Recalled for Sterility Assurance Concerns
Prodimed Plastimed Division is recalling 7,220 Combicath catheters for mini bronchoalveolar lavage due to a lack of assurance of sterility.
Product
Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 60 cm x 2.7 mm Product Code: 58216 27US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2523-2020·2020-07-15
Philips EasyDiagnost Eleva DRF X-ray System Recalled for Power Supply Defect
Philips is recalling 52 EasyDiagnost Eleva DRF X-ray systems because incorrectly installed thermo switches in the main power supply may cause malfunction.
Product
EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2527-2020·2020-07-15
TeDan Phantom CS Distraction Screw Recalled for Lack of Pouch Seal
TeDan Surgical Innovations is recalling 1,965 sterile Phantom CS Distraction Screws because the packaging lacks a pouch seal, compromising the sterile claim.
Product
PHANTOM CS DISTRACTION SCREW, 14 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2530-2020·2020-07-15
TeDan Phantom CS Quick Start Distraction Screw Recall for Seal Defect
TeDan Surgical Innovations LLC is recalling 340 sterile Phantom CS Quick Start Distraction Screws due to a lack of pouch seal.
Product
PHANTOM CS QUICK START DISTRACTION SCREW, 16 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2524-2020·2020-07-15
TeDan 3COR Distraction Screw Recall Due to Sterility Seal Failure
TeDan Surgical Innovations LLC is recalling 3COR Distraction Screws because the pouch seal is lacking, compromising the sterile labeling.
Product
3COR DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2537-2020·2020-07-15
Vitalconnect VistaSolution Software Recall for Missing SpO2 Notifications
Vitalconnect Inc. is recalling VistaSolution software due to a defect that prevented low SpO2 alerts, potentially exposing patients to short-term hypoxia.
Product
VistaSolution, physiological signal transmitter. A software graphical user interface for use by healthcare professionals to display physiological data collected by the wireless remote monitoring system in healthcare settings. This is a secondary, adjunct patient monitor and is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2490-2020·2020-07-15
Prodimed Combicath catheters recalled due to sterility assurance concerns
Prodimed is recalling 1,460 Combicath catheters nationwide because the company cannot assure the products are sterile.
Product
Prodimed Combicath catheters for blind or fibrescope-guided protected distal bronchial sampling (PDBS)- COMBICATH PE 90 cm Product Code: 58229 19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2526-2020·2020-07-15
TeDan Phantom CS Distraction Screw Recall for Lack of Pouch Seal
TeDan Surgical Innovations LLC is recalling 1,965 Phantom CS Distraction Screws because the packaging lacks a pouch seal, compromising the sterile labeling.
Product
PHANTOM CS DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2521-2020·2020-07-15
United Imaging Recalls uDR 596i Digital Medical X-Ray Imaging Systems
Shanghai United Imaging Healthcare is recalling six uDR 596i digital medical X-ray systems due to software errors that may cause incorrect anatomical positioning or loss of image tags, leading to additional radiation exposure.
Product
uDR 596i Digital Medical X-Ray Imaging System - Product Usage: intended to use by a qualified/ trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, limbs and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2488-2020·2020-07-15
Prodimed Combicath Catheters Recalled Due to Sterility Assurance Concerns
Prodimed Plastimed Division is recalling Combicath catheters for mini bronchoalveolar lavage because of a lack of assurance of sterility.
Product
Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2020·2020-07-15
Radiometer ABL800 FLEX Blood Gas Analyzer Software Recall
Radiometer Medical ApS is recalling ABL800 FLEX blood gas analyzers due to a software issue that may cause patient mix-ups.
Product
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-801; UDI (01)05700693938011. Model 393-801 is available as ABL837. The FlexQ module is optional and can be added to all models and configurations.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-2531-2020·2020-07-15
Philips M3015A Microstream CO2 Extension Recall for Incompatibility
Philips is recalling M3015A Microstream CO2 Extensions because they are incompatible with IntelliVue X3 and MMX monitors, which may cause a loss of monitoring.
Product
Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monitor (Model No. 867030) or a lntelliVue MMX Multi-Measurement Module (Model No. 867036)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2542-2020·2020-07-15
KCI ACTIV.A.C Therapy System Recalled for Unexpected Power Off
KCI USA is recalling ACTIV.A.C Therapy Systems because they may power off without warning, stopping negative pressure wound therapy.
Product
ACTIV.A.C Therapy System; Model Numbers; US: 340000 ACTIV.A.C., NORTH AMERICAN UDI (01)00878237008188 - Product Usage: is an integrated wound management system for use in the acute, extended, and home care settings. When used on open wounds, it is intended to create an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2545-2020·2020-07-15
Centurion Difficult IV Kit Recalled for False Carboxyhemoglobin Results
Centurion Medical Products is recalling 140 Difficult IV Kits containing BD Vacutainer tubes that may cause false carboxyhemoglobin results.
Product
Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium Heparin Tubes (BD Vacutainer-BD Codes 367884 & 367960; Centurion code 45177 (VACUTAINER GREEN TOP) and 84815 (VACUTAINER 3ML LT. GREEN). Centurion Kit Code: IV8860
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2532-2020·2020-07-15
Bound Tree Medical Recalls Ambu King LTS-D Supraglottic Airway Kits
Bound Tree Medical is recalling 167 Ambu King LTS-D Supraglottic Airway Kits because they contain an incompatible catheter-tip syringe that may prevent the airway balloon from inflating properly.
Product
Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Part Number: KLTSD404K Curaplex Ambu¿ King LTS-D" Supraglottic Airway Kit with ET Tube (hereafter the Kit which contains all of the components necessary to successfully obtain an open patient airway with an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2493-2020·2020-07-15
Radiometer ABL800 FLEX Blood Gas Analyzers Recalled for Software Issues
Radiometer Medical ApS is recalling ABL800 FLEX blood gas analyzers due to a software issue that creates a potential risk of patient mix-up.
Product
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model 393-800 is available in the following configurations: ABL835, ABL830, ABL827, ABL825, ABL825, ABL820, ABL817, ABL815, ABL810, ABL805 and ABL810 BG only and…
Category
Medical Device
Distribution
46 states
HighNHTSA·20V410000·2020-07-15
Toyota Recalls 2018-2020 Tundra for Dim Turn Signals
Toyota is recalling 2018-2020 Tundra trucks with LED headlights because a wiring error causes front turn signals to flash too dimly, potentially increasing crash risk.
Product
TOYOTA — TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2544-2020·2020-07-15
Cardinal Health NPWT Canisters Recalled Due to Oversized O-Ring Defect
Cardinal Health is recalling 1,960 NPWT Occlusion Detection Canisters because an oversized O-ring may prevent proper installation into the device connector.
Product
Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and…
Category
Medical Device
Distribution
Distributed nationwide