State

Louisiana product recalls

73,092 recalls have nationwide distribution and so reach Louisiana. 6,958 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,958
Critical: 1,109
Severe: 1,497
Most recent: 2026-09-23

Of the 6,958 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,497 (22%) are Severe.

Which agencies issued them

These figures cover only the 6,958 recalls whose distribution notice names Louisiana specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10026–10050 of 80050

HighFDA (Devices)·Z-3256-2024·2024-10-02
Biodesign Fistula Plug Implant Recalled for Premature Expiration
Cook Biotech is recalling the Biodesign Fistula Plug implant because devices expire before their labeled expiration dates. Thirty-nine units distributed worldwide are affected.
Product
Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G46372
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3250-2024·2024-10-02
Cook Biotech Biodesign Fistula Plug implants recalled for premature expiration
Cook Biotech is recalling Biodesign Fistula Plug C-FPB-0.4 implants because products expire before their printed expiration dates.
Product
Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G24667
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3260-2024·2024-10-02
Biodesign Recto-Vaginal Fistula Plug Recalled for Premature Expiration
Cook Biotech is recalling 8 units of Biodesign Recto-Vaginal Fistula Plug devices because they expire before the date printed on the label. The affected products may lose sterility if used after actual expiration.
Product
Biodesign Recto-Vaginal Fistula Plug RVP-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal fistulas. Order Number (GPN): G46603
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3158-2024·2024-10-02
Mobile X-Ray System Exposure Settings May Not Apply Correctly
Fujifilm mobile x-ray systems may fail to apply configured exposure settings or default to adult chest imaging parameters. This could result in inappropriate radiation exposure levels.
Product
The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3232-2024·2024-10-02
Medical Device Kit Recall: Sterilization Assurance Cannot Be Confirmed
American Contract Systems is recalling 60 Shoulder SESH18I medical convenience kits nationwide due to equipment failure that resulted in out-of-specification humidity readings, preventing sterilization assurance confirmation.
Product
Shoulder, SESH18I; Medical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3300-2024·2024-10-02
Custodiol HTK Solution Recalled for Potential Particle Contamination
Custodiol HTK Solution is subject to a Class II recall due to the potential for particles in the solution. The affected product consists of 48 cartons distributed in North Carolina.
Product
Custodiol HTK Solution, 500ml bottle. 10 per carton.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3219-2024·2024-10-02
Karl Storz Hopkins Telescope Recalled for Unapproved Reprocessing Instructions
Karl Storz Hopkins Telescope 6 endoscopes are being recalled because the instructions for use contain reprocessing procedures not reviewed or approved by the FDA. Affected units should not be used until corrected instructions are provided.
Product
Karl Storz - Endoskope , REF: 27093AA Hopkins Telescope 6, Rx only, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3227-2024·2024-10-02
Endovascular AAA Packs Recalled Due to Sterilization Process Defect
American Contract Systems is recalling 93 units of Endovascular AAA Packs due to inability to confirm sterilization assurance requirements were met following an environmental monitoring failure.
Product
Endovascular AAA Pack, ESED52B; Medical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0662-2024·2024-10-02
Sunscreen product recalled for microbial contamination nationwide
SHEET SPF 30 Mineral sunscreen is being recalled for microbial contamination. The product was distributed nationwide.
Product
SHEET SPF 30 MINERAL — SHEET SPF 30 MINERAL (TITANIUM DIOXIDE, ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3210-2024·2024-10-02
AVS Anchor-C Cervical Cage Instructions for Use Labeling Correction
Stryker Spine recalled the electronic Instructions for Use revision 5 for the AVS Anchor-C Cervical Cage System because specific indications language for the US and Canada was inadvertently removed.
Product
AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3225-2024·2024-10-02
Karl Storz Nephroscope Recall Due to Unapproved Reprocessing Instructions
Karl Storz Endoscope nephroscopes (REF: 27840KA) are being recalled because their instructions for use contain reprocessing methods that have not been reviewed or approved by the FDA for safety and efficacy.
Product
Karl Storz - Endoskope , REF: 27840KA, Nephroscope for MIP L, Rx only, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3254-2024·2024-10-02
Cook Biotech Recalls Biodesign Fistula Plug Due to Early Expiration
Cook Biotech, Inc. is recalling 102 units of Biodesign Fistula Plug C-FPS-0.7 because the products expire prior to the date printed on the labeling.
Product
Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G54614
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3253-2024·2024-10-02
Cook Biotech Recalls Biodesign Fistula Plugs Due to Expiration Date Errors
Cook Biotech is recalling 93 Biodesign Fistula Plugs because the products expire prior to the expiration date printed on the labeling.
Product
Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G54613
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3188-2024·2024-10-02
CooperSurgical Recalls Silver-Plated Copper Sims Uterine Sound for Incorrect Marking
CooperSurgical is recalling 468 units of Silver-Plated Copper Sims Uterine Sounds because they were laser-marked with the incorrect part number during manufacturing.
Product
Silver-Plated Copper Sims Uterine Sound, Part Number 64-600
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3189-2024·2024-10-02
Stainless Steel Sims Uterine Sound Recalled for Incorrect Part Number
CooperSurgical, Inc. is recalling the Stainless Steel Sims Uterine Sound (Part Number 64-601) because some units were laser-marked with incorrect part numbers during manufacturing. No injuries have been reported.
Product
Stainless Steel Sims Uterine Sound, Part Number 64-601
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3196-2024·2024-10-02
Philips Ingenia 3.0T CX MRI Machine Carrier Assembly Screws May Loosen
Philips Ingenia 3.0T CX MRI machines may have loose screws in the RF carrier assembly that could protrude and interfere with the tabletop mechanism, potentially delaying patient scans.
Product
Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782105
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3261-2024·2024-10-02
Biodesign Inguinal Hernia Graft Recall Due to Premature Expiration
Cook Biotech is recalling Biodesign Inguinal Hernia Graft units because products expire before their labeled expiration date, potentially affecting surgical outcomes.
Product
Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3220-2024·2024-10-02
Karl Storz Hopkins Telescope 6 endoscope recalled for unapproved reprocessing instructions
Karl Storz is recalling the Hopkins Telescope 6 endoscope because its Instructions for Use contain reprocessing procedures that have not been FDA-reviewed or approved. The recall affects 1,982 units distributed nationwide.
Product
Karl Storz - Endoskope , REF: 27292AMA, Hopkins Telescope 6, Rx only, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V732000·2024-10-01
2021-2024 Porsche Taycan battery short circuit fire risk
Porsche is recalling 2021-2024 Taycan vehicles due to high-voltage battery short circuits that increase fire risk. Dealers will install diagnostic software and replace batteries as needed, advising owners to charge only to 80% capacity until repairs are completed.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V736000·2024-10-01
2025 Daimler Trucks Fuel Pump Barrel Fracture Recall
Daimler Trucks North America is recalling certain 2025 commercial trucks with Cummins fuel pumps that may fracture and leak fuel, potentially causing engine stall. No injuries have been reported.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 49X, CASCADIA, XCM, XCP
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V730000·2024-10-01
Porsche Recalls 2025 Taycan for Delayed Rearview Camera Display
Porsche is recalling 2025 Taycan vehicles because the rearview camera image may not display immediately when shifting into reverse, increasing crash risk.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V734000·2024-10-01
2025 International HX and LT vehicles recalled for fuel pump fracture risk
Navistar is recalling 2025 International HX and LT vehicles with Cummins X15 diesel engines due to fuel pump barrel fracture risk. The fracture can cause fuel leaks and engine stalls, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL HX, LT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V731000·2024-10-01
2020-2023 Porsche Taycan Recalled for High-Voltage Battery Short Circuit Risk
Porsche is recalling 2020-2023 Taycan vehicles due to a potential short circuit in the high-voltage battery that increases fire risk. Owners should limit charging to 80% until dealers replace the affected battery modules.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E082000·2024-10-01
Chrysler Recalls Steering Column Modules for Turn Signal Defect
Chrysler is recalling specific MOPAR steering column control modules because the turn signal self-canceling feature may not function properly, increasing crash risk.
Product
EXTERIOR LIGHTING:TURN SIGNAL recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V729000·2024-10-01
Ram 1500 Recalled for Turn Signal Self-Canceling Defect
Chrysler is recalling 2023-2024 Ram 1500 vehicles because the turn signal self-canceling feature may not function properly, increasing crash risk.
Product
RAM — RAM 1500
Category
Vehicle
Distribution
Distributed nationwide