State

Louisiana product recalls

73,824 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,966
Critical: 1,107
Severe: 1,740
Most recent: 2026-11-04

Of the 6,966 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,740 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48376–48400 of 80790

ModerateFDA (Devices)·Z-1521-2017·2017-03-29
BioMerieux Recalls ETEST Ceftazidime Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Ceftazidime TZ256 strips because their shelf-life claims are not supported by internal testing.
Product
ETEST Ceftazidime TZ256 Foam packaging, Product Name: ETEST Ceftazidime TZ 0.016-256. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1541-2017·2017-03-29
Hitachi Echelon Oval MRI System Recalled for Image Data Errors
Hitachi Medical Systems America Inc is recalling 25 Hitachi Echelon Oval MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
Product
Hitachi Echelon Oval MRI System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1500-2017·2017-03-29
Haag-Streit EyeSuite Software Recalled for Potential Patient Data Misattribution
Haag-Streit USA Inc is recalling EyeSuite i.8.2.1.0 software due to a risk that patient data may be stored under the wrong patient on the DICOM Server.
Product
EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra Ocular Lenses (IOLs).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1486-2017·2017-03-29
Merge Healthcare Recalls Cardio Software Due to STAT Study Display Issue
Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because the study list fails to display STAT studies without a manual refresh.
Product
Merge Cardio software.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1542-2017·2017-03-29
Hitachi Echelon MRI System Recalled for Image Data Transfer Errors
Hitachi Medical Systems America Inc is recalling 68 Hitachi Echelon MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
Product
Hitachi Echelon MRI System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1533-2017·2017-03-29
Siemens Syngo.plaza PACS Systems Recalled for Software Update Issues
Siemens Medical Solutions is recalling 13 Syngo.plaza PACS systems nationwide due to software update issues. The recall is voluntary and has been terminated.
Product
Syngo.plaza, Picture Archiving and Communications System (PACS) Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1532-2017·2017-03-29
BioMerieux Recalls ETEST Ceftriaxone Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Ceftriaxone strips because their shelf-life claims are not supported by internal testing. The products were distributed worldwide.
Product
ETEST Ceftriaxone TXL32 FOAM packaging, Product Name: ETEST Ceftriaxone TX 0.002-32(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0612-2017·2017-03-29
Fougera Recalls Desonide Ointment Tubes Due to Labeling Mixup
Fougera Pharmaceuticals is recalling 14,665 tubes of Desonide Ointment because unit boxes may contain tubes labeled as Ketoconazole Cream.
Product
Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1493-2017·2017-03-29
Philips Recalls Brilliance BigBore CT Scanners Due to Image Reconstruction Error
Philips is recalling 67 Brilliance BigBore CT scanners because 4D CT images may be reconstructed at a single phase while incorrectly labeled as specific phases.
Product
Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display…
Category
Medical Device
Distribution
22 states
ModerateFDA (Devices)·Z-1522-2017·2017-03-29
BioMerieux Recalls ETEST Cephalothin CE 256 Foam Packaging Due to Stability Issues
BioMerieux SA is recalling ETEST Cephalothin CE 256 Foam packaging because current shelf-life claims are not supported by internal testing.
Product
ETEST Cephalotin CE 256 Foam packaging, Product Name: ETEST Cephalothin CE 0.016-256. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1495-2017·2017-03-29
Zimmer Biomet Recalls Orthosize Templating Software Due to Incorrect Files
Zimmer Biomet is recalling Orthosize Templating Version 1.2.6 digital templates because they were created with incorrect files, affecting preoperative planning for orthopedic surgery.
Product
Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates. For preoperative planning of orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1530-2017·2017-03-29
BioMerieux Recalls ETEST Gentamicin Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Gentamicin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Product
ETEST Gentamicin GM256 FOAM packaging, Product Name: ETEST Gentamicin GM 0.016-256(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0611-2017·2017-03-29
Sun Pharmaceutical Recalls Testosterone Cypionate Injection Due to Particulate Matter
Sun Pharmaceutical Industries, Inc. is recalling 83,188 vials of Testosterone Cypionate Injection due to the presence of particulate matter.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1526-2017·2017-03-29
BioMerieux Recalls ETEST Doripenem Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Doripenem DOR32 FOAM packaging strips because internal testing does not support the current shelf-life claims.
Product
ETEST Doripenem DOR32 FOAM packaging, Product Name: Etest Doripenem DOR 0.002-32. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1535-2017·2017-03-29
Tearscience LipiFlow System Recalled for Inconsistent Storage Temperature Labeling
Tearscience is recalling LipiFlow Thermal Pulsation Systems because the labeled storage temperature does not match tested conditions for the full shelf life.
Product
LipiFlow Thermal Pulsation System/LipiFlow, System Activator (Disposable), Rx Only, Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1529-2017·2017-03-29
BioMerieux Recalls ETEST Imipenem IP32 Foam Packaging Due to Stability Issues
BioMerieux SA is recalling ETEST Imipenem IP32 Foam packaging because the current shelf-life claims are not supported by internal testing.
Product
ETEST Imipenem IP32 Foam packaging, Product Name: ETEST Imipenem IP 0.002-32. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1484-2017·2017-03-29
FDA Recalls Microbore Extension Sets Due to Incorrect Priming Volume Labeling
Vygon MFG is recalling 30,700 AMS-636 Microbore extension sets because the package displays an incorrect priming volume.
Product
AMS-636, 60" Microbore extension set. Product Usage: Accessory devices used to administer medical fluids.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1531-2017·2017-03-29
BioMerieux Recalls ETEST Tobramycin Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Tobramycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Product
ETEST Tobramycin TM256 FOAM packaging, Product Name: ETEST Tobramycin TM 0.016-256(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1525-2017·2017-03-29
BioMerieux Recalls ETEST Vancomycin Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Vancomycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Product
ETEST Vancomycin VA 256 FOAM packaging, Product Name: ETEST Vancomycin VA 0.016-256. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1527-2017·2017-03-29
BioMerieux Recalls Etest Benzyl Penicillin Strips Due to Stability Issues
BioMerieux SA is recalling Etest Benzyl Penicillin PG256 FOAM packaging because shelf-life claims are not supported by internal testing.
Product
ETEST Benzyl Penicillin PG256 FOAM packaging, Product Name: Etest Benzylpenicillin PG 0.016-256 (high). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1492-2017·2017-03-29
Philips CT Scanner Recall for Incorrect 4D CT Image Phase Annotations
Philips is recalling 11 Brilliance BigBore Oncology CT scanners because retrospective 4D CT scans may display incorrect phase annotations.
Product
Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display…
Category
Medical Device
Distribution
22 states
ModerateFDA (Devices)·Z-1524-2017·2017-03-29
BioMerieux Recalls ETEST Ciprofloxacin CI 32 Foam Due to Stability Issues
BioMerieux SA is recalling ETEST Ciprofloxacin CI 32 Foam products because their shelf-life claims are not supported by internal testing.
Product
Ciprofloxacin CI 32 Foam packaging, Product Name: ETEST Ciprofloxacin CI 0.002-32. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0610-2017·2017-03-29
AvKARE Recalls Famciclovir Tablets Due to Impurity Levels
AvKARE Inc. is recalling 116 cartons of 500 mg Famciclovir tablets because the product exceeded specifications for unknown impurities.
Product
Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1523-2017·2017-03-29
BioMerieux Recalls ETEST Ceftriaxone Strips Due to Stability Issues
BioMerieux SA is recalling ETEST Ceftriaxone antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Product
ETEST¿ Ceftriaxone TXL32 SPB, Product Name: ETEST¿ Ceftriaxone TX 0.002-32(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1519-2017·2017-03-29
Teleflex Recalls Non-Latex Nasopharyngeal Airways Due to Labeling Error
Teleflex Medical is recalling 7,600 units of Green Non-Latex Robertazzi Nasopharyngeal Airways due to a labeling error. The voluntary recall covers products distributed in the US, Canada, and Mexico.
Product
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.
Category
Medical Device
Distribution
Distributed nationwide