State

Alabama product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2526–2550 of 79260

HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2026·2026-04-08
Oxoid Microbact Listeria kit may identify the incorrect organism
Oxoid, part of Thermo Fisher Scientific, is recalling one lot of the Microbact 12L Listeria identification kit because it may identify the incorrect organism.
Product
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2026·2026-04-08
Burlington Medical kilts may lose radiation attenuation over time
Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Kilt
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1695-2026·2026-04-08
Olympus SOLTIVE Pro laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Pro SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1687-2026·2026-04-08
Artoura ultra high profile expander infusion needles may be blunt
Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1760-2026·2026-04-08
Burlington Medical caps may lose radiation attenuation over time
Burlington Medical is recalling protective caps made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Caps.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2026·2026-04-08
Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments
Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1680-2026·2026-04-08
Philips Azurion 5 M20 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2026·2026-04-08
Artoura breast tissue expander infusion set needles may be blunt
Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V222000·2026-04-08
Toyota Recalls Lexus RC, GS, and IS Models for Fuel Pump Failure
Toyota is recalling specific Lexus RC, GS, and IS models because a failing fuel pump can cause the engine to stall, increasing crash risk.
Product
LEXUS — LEXUS RC, GS, IS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0409-2026·2026-04-08
Quality Choice irritation relief eye drops recalled over sterility assurance
Quality Choice Eye Drops Irritation Relief, containing tetrahydrozoline HCl and zinc sulfate, are being recalled for lack of assurance of sterility. 182,424 bottles are affected.
Product
QUALITY CHOICE EYE DROPS IRRITATION RELIEF — QUALITY CHOICE EYE DROPS IRRITATION RELIEF (TETRAHYDROZOLINE HCL, ZINC SULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0415-2026·2026-04-08
Rugby and Walgreens lubricant eye drops recalled over sterility assurance
K.C. Pharmaceuticals is recalling Sterile Eye Drops Soothing Tears, sold as Rugby Lubricating Eye Drops and Walgreens Lubricant Eye Drops, for lack of assurance of sterility.
Product
STERILE EYE DROPS SOOTHING TEARS (polyethylene glycol 400 0.4% and propylene glycol 0.3%), 0.5 OZ 0.5 fl oz (15 mL) bottles; a) Rugby LUBRICATING EYE DROPS, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1219-94; b) Walgreens, Lubricant Eye Drops, DISTRIBUTED BY
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2026·2026-04-08
Philips Allura Xper FD20/15 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15; System Code: 722058;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1703-2026·2026-04-08
VOLT bone taps swapped between lots carry the incorrect thread
The 2.4 VOLT Tap Cortex Screw is being recalled after a full lot swap with the VOLT Locking Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2026·2026-04-08
Philips Allura Xper FD10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0421-2026·2026-04-08
Prazosin hydrochloride further lots recalled over nitrosamine impurity levels
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1685-2026·2026-04-08
Artoura textured tissue expander infusion set needles may be blunt
Mentor is recalling textured Artoura Breast Tissue Expanders with integral injection dome because the infusion sets may contain a dull or blunt needle tip.
Product
Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1688-2026·2026-04-08
Stryker surgical light assembly may not support the ceiling cover weight
Stryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System because the light assembly may not adequately support the weight of the ceiling cover.
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2026·2026-04-08
MiniMed 670G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0412-2026·2026-04-08
Leader ultra lubricating eye drops recalled over sterility assurance failure
Leader Ultra Lubricating Eye Drops, containing polyethylene glycol 400 and propylene glycol, are being recalled for lack of assurance of sterility.
Product
LEADER ULTRA LUBRICATING EYE DROPS — LEADER ULTRA LUBRICATING EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1745-2026·2026-04-08
MiniMed 720G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2026·2026-04-08
Monoject tuberculin syringe packages actually contain U-100 insulin syringes
Cardinal Health is recalling two lots of Monoject Tuberculin Syringes because the packaging identifies them as 1 mL Luer Lock tuberculin syringes but the contents are U-100 insulin syringes.
Product
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1744-2026·2026-04-08
MiniMed 700G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 700G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide