State

Alabama product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51326–51350 of 80211

HighFDA (Devices)·Z-2673-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 2,574 diamond coated tips and burs because the labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2016·2016-09-07
Cardinal Health Recalls Arterial Blood Gas Kits Missing Safety Clasp
Cardinal Health is recalling specific lots of 9025TRU Arterial Blood Gas Kits because they are missing a locking clasp component, posing a potential safety risk.
Product
The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2709-2016·2016-09-07
Merge Cardio software recall due to incorrect patient data saving
Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because reports may be saved to incorrect patient records.
Product
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Image processing system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V645000·2016-09-07
Forest River Recalls 2017 Coachmen Viking Trailers Due to Roof Strut Defect
Forest River is recalling 2017 Coachmen Viking recreational trailers because a missing wire clip may allow the roof strut to detach, causing the roof to drop and increasing injury risk.
Product
COACHMEN — COACHMEN VIKING
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16T014000·2016-09-07
Tireco Recalls Milestar Tires with Incorrect Sidewall Markings
Tireco is recalling specific Milestar BS623 tires with incorrect sidewall markings that may lead to overloading and tire failure.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2691-2016·2016-09-07
Elekta Recalls HexaPOD evo RT Systems for Positioning Errors
Elekta is recalling 13 HexaPOD evo RT Systems because the treatment couch may not move fully to the correct 3D position, potentially leading to unrecognized positioning errors during radiotherapy.
Product
HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate patient positioning with assistance of a 3D Tracking System in a radiotherapy environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2689-2016·2016-09-07
Mindray A7 Anesthesia Delivery System Recalled for Potential Oxygen Leak
Mindray is recalling 167 A7 Anesthesia Delivery Systems due to a potential leak on the back-up oxygen and air cylinder yokes.
Product
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16C007000·2016-09-07
Evenflo Recalls Evolve 3-in-1 Booster Seats Due to Harness Loosening Risk
Evenflo is recalling specific Evolve 3-in-1 Combination Booster Seats because children can access a button to loosen the harness, increasing injury risk in a crash.
Product
CHILD SEAT:HARNESS:STRAP/WEBBING recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2016·2016-09-07
Philips Recalls UNIQ 1.0 Fluoroscopy Systems Due to Power Supply Failures
Philips is recalling 1,536 UNIQ 1.0 fluoroscopy systems because certain low-voltage DC power supplies have an increased failure rate.
Product
UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table, 722033; UNIQ FD10/10 OR Table, 722034; UNIQ FD20 OR Table, 722035; UNIQ FD20/20, 722038; UNIQ FD20/20 biplane OR Table, 722039; UNIQ FD20/15, 722058…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2672-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 30,719 diamond coated tips and burs because labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX, VARIOS 150). The intended use of the tips is based on the parent device. For the ultrasonic scalers and the sonic air scaler, the tips are used for various…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2674-2016·2016-09-07
Nakanishi Diamond Coated Dental Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 4,284 diamond coated dental tips because the packaging failed to indicate they are single-use only, posing a risk of cross-contamination.
Product
Diamond Coated Tips and Burs are accessories to the air powered dental handpiece (S-MAX pico) The intended use of the tips is based on the parent device. For burs used with the dental handpieces, the intended use is general dental actions such as removing carious material…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2669-2016·2016-09-07
Philips Recalls Allura Xper Systems Due to Power Supply Failure Risk
Philips is recalling 1,536 Allura Xper medical imaging systems because certain low-voltage DC power supplies have an increased failure rate.
Product
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; Allura Xper FD20 OR Table, 722035; Allure Xper…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2705-2016·2016-09-07
Medical Vision Ab Recalls Double Pump RF Patient Cassettes
Medical Vision Ab is recalling 3,295 Double Pump RF Patient Cassettes because sterile package breakage may compromise device sterility.
Product
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.
Category
Medical Device
Distribution
22 states
ModerateFDA (Drugs)·D-1474-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2706-2016·2016-09-07
Terumo Cardiovascular Procedure Kits Recalled for Incorrect Tubing Coating Labeling
Terumo is recalling 2,207 cardiovascular procedure kits because they are labeled as containing coated tubing but actually contain non-coated tubing.
Product
Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled containing Coated Tubing as follows: This product is intended for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it. This product is a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1475-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1477-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1478-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2711-2016·2016-09-07
Nidek Specular Microscope CEM-530 Software Recall for Unapproved Feature
Nidek Inc is recalling 29 Specular Microscope CEM-530 units because software versions 1.08 and 1.09 include an unapproved analysis feature.
Product
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides non-contact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of…
Category
Medical Device
Distribution
18 states
LowFDA (Drugs)·D-1473-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1476-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V640000·2016-09-06
Acura Recalls 2015 TLX Vehicles for Transmission Wire Harness Defect
Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.
Product
ACURA — ACURA TLX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V641000·2016-09-06
Audi Recalls 2017 Q7 Vehicles for Third-Row Seat Back Defect
Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V643000·2016-09-06
Ford Recalls Multiple Models Due to Door Latch Defect
Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.
Product
FORD — FORD, LINCOLN ESCAPE, TRANSIT CONNECT, MKC, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V644000·2016-09-06
Mazda Recalls Vehicles Due to Corroded Lift Gate Support Struts
Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.
Product
MAZDA — MAZDA MAZDASPEED3, MAZDA3, MAZDA5, CX-5
Category
Vehicle
Distribution
Distributed nationwide