State

Louisiana product recalls

72,968 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,922
Critical: 1,094
Severe: 1,483
Most recent: 2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6026–6050 of 79890

HighFDA (Devices)·Z-2174-2025·2025-08-06
HeartSine samaritan public access defibrillators may not deliver shocks properly
HeartSine SAM 350P, 360P and 450P public access defibrillators are being recalled because a component manufacturing issue means the device may not function properly to deliver shocks. 190,516 units affected.
Product
HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access Defibrillator)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2217-2025·2025-08-06
SmartPath to Ingenia Elition X gradient coils may overheat
SmartPath to Ingenia Elition X systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 33 units affected.
Product
SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2199-2025·2025-08-06
SwabFlush prefilled syringes carry SwabCaps with a compromised seal
SwabFlush Prefilled Syringes with ICU Medical SwabCaps are being recalled because a manufacturing issue affects the SwabCap seal, which may reduce disinfection of the luer access valve. 1,427,100 units affected.
Product
SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2218-2025·2025-08-06
Philips MR 7700 upgrade gradient coils may act as a heat source
Upgrade to MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 26 units are affected.
Product
Upgrade to MR 7700 Model Number (REF): 782130;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2213-2025·2025-08-06
Philips MR 5300 gradient coils may act as a heat source
MR 5300 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 551 units are affected.
Product
MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2177-2025·2025-08-06
HarmonyAIR dual flat panel monitor yokes may detach from spring arm
Dual Flat Panel Monitor accessories for HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 167 units are affected.
Product
Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0544-2025·2025-08-06
Bicillin L-A penicillin vials recalled after particulates found during visual inspection
Bicillin L-A (penicillin G benzathine injectable suspension) 1,200,000 units per 2 mL is being recalled because of CGMP deviations, with particulates identified during visual inspection. 50,855 vials affected.
Product
BICILLIN L-A — BICILLIN L-A (PENICILLIN G BENZATHINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2222-2025·2025-08-06
Osteotec silicone finger implants may contain foreign material
Osteotec Silicone Finger Implants in sizes 3, 4 and 5 are being recalled because there is the potential that the silicone implant may contain foreign material. 15,573 units are affected.
Product
Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant Model/Catalog Number: OSTF-3 (Sz. 3), OSTF-4 (Sz. 4), OSTF-5 (Sz. 5) Software Version: N/A Product Description: The Osteotec Silicone Finger Implant is a one-piece, sterile, flexible silicone elastomer implan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2203-2025·2025-08-06
Philips Evolution Upgrade 3.0T gradient coils may act as heat source
Evolution Upgrade 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 50 units are affected.
Product
Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2175-2025·2025-08-06
Inseego dongle kit flash drives carry outdated patient monitor software
Inseego USB8 4G Dongle Kits for the Tempus Pro Monitor are being recalled because the kit's USB flash drive contains outdated software that could revert the monitor and reintroduce a previous issue. 55 units affected.
Product
Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2207-2025·2025-08-06
Philips Ingenia 3.0T CX gradient coils may act as heat source
Ingenia 3.0T CX MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 350 units are affected.
Product
Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2234-2025·2025-08-06
LVP primary administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Single Outlet Low Sorbing, are being recalled because of the potential for external cassette leaks. 35,925 units are affected.
Product
LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25). Product Code: SET-0021-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2224-2025·2025-08-06
Strep Selective II Agar plates may carry Listeria monocytogenes contamination
Strep Selective II Agar, product number R01859, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 371 units are affected.
Product
Strep Selective II Agar, Product Number R01859
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2208-2025·2025-08-06
Philips Ingenia Ambition S gradient coils may act as heat source
Ingenia Ambition S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 611 units are affected.
Product
Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2025·2025-08-06
Philips MR 7700 gradient coils may act as a heat source
MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 82 units are affected.
Product
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2216-2025·2025-08-06
SmartPath to dStream XR gradient coils may act as heat source
SmartPath to dStream for XR and 3.0T systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 294 units affected.
Product
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2025·2025-08-06
LVP dual-inlet administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site, are being recalled because of the potential for external cassette leaks. 19,225 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2206-2025·2025-08-06
Philips Ingenia 3.0T gradient coils may act as a heat source
Ingenia 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 1,467 units are affected.
Product
Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2025·2025-08-06
LVP blood administration sets have potential for external cassette leaks
LVP Blood Products Administration Sets are being recalled because of the potential for external cassette leaks. 14,280 units are affected.
Product
LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2204-2025·2025-08-06
Philips Ingenia 1.5T gradient coils may act as a heat source
Ingenia 1.5T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 2,279 units are affected.
Product
Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2189-2025·2025-08-06
Philips Allura R8.2.x systems may temporarily lose x-ray imaging functionality
Philips Allura R8.2.x systems are being recalled because of the potential for temporary loss of imaging (X-ray) functionality due to a software issue. 4,508 units are affected.
Product
Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper FD10/10, Model Number: 722027. 3. Allura Xper FD20, Model Number: 722028. 4. Allura Xper FD20/10, Model Number: 722029. 5. Allura Xper FD10 OR Table,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2201-2025·2025-08-06
Philips Achieva XR gradient coils may act as a heat source
Achieva XR MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 40 units are affected.
Product
Achieva XR; Model Numbers (REF): (1) 781153, (2) 781253;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2212-2025·2025-08-06
Philips MRI Machine Intera 3.0T Quasar Dual Recalled for Fire Risk
Philips is recalling its Intera 3.0T Quasar Dual MRI system due to a potential fire hazard from gradient coil failures. The recall affects one unit distributed worldwide.
Product
Intera 3.0T Quasar Dual Model Number (REF): 781150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2209-2025·2025-08-06
Philips Ingenia Ambition X gradient coils may act as heat source
Ingenia Ambition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 690 units are affected.
Product
Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2198-2025·2025-08-06
CoSense sampling sets may carry residual carbon monoxide from insufficient aeration
Precision Sampling Sets for the CoSense End-Tidal Carbon Monoxide Monitor are being recalled because residual carbon monoxide may remain in the cannula filter, which may raise ETCOc scores. 2,160 units affected.
Product
Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor
Category
Medical Device
Distribution
Distributed nationwide