State

Louisiana product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50601–50625 of 80793

SevereFDA (Devices)·Z-0055-2017·2016-10-26
Vascular Solutions Recalls Twin-Pass Dual Access Catheters Due to Manufacturing Residue
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.
Product
Vascular Solutions Twin-Pass .023" Dual Access Catheter, model 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V778000·2016-10-26
Ford Recalls 2017 F-Series Trucks Due to Fuel Leak Fire Risk
Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.
Product
FORD — FORD F-550 SD, F-350 SD, F-450 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0044-2017·2016-10-26
Teleflex Medical Recalls Willy Rusch Tracheostomy Tube Sets
Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.
Product
Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0180-2017·2016-10-26
Windstone Medical Packaging Recalls Endoscopy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.
Product
Endoscopy Pack, Kit number PSS1646 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2017·2016-10-26
RTI Surgical Recalls Streamline OCT Spinal Rods Due to Cracks
RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.
Product
RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3), the Streamline OCT Occipito-Cervico-Thoracic System is…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0118-2017·2016-10-26
Awareness Boost Tea Recalled for Potential Salmonella Contamination
Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.
Product
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness Corporation P.O. Box 2289 Chandler, AZ 85244
Category
Food
Distribution
33 states
SevereFDA (Devices)·Z-0185-2017·2016-10-26
Windstone Medical Packaging Recalls Extremity Tray Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Extremity Tray, Kit number AMS1200(B and AMS1200(C convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0127-2017·2016-10-26
X Spine Systems Recalls Calix T PEEK Lumbar System Trial Devices
X Spine Systems is recalling 1,186 Calix T PEEK Lumbar System trial devices because components may detach and lodge in the intervertebral space during surgery.
Product
Calix T PEEK Lumbar System, TLIF Trial
Category
Medical Device
Distribution
19 states
SevereFDA (Devices)·Z-0233-2017·2016-10-26
Windstone Medical Packaging Recalls Major Laparotomy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Major Laparotomy Pack - NS, kit number AMS4347 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0126-2017·2016-10-26
X Spine Systems Recalls Calix T PEEK Lumbar System TLIF Rasps
X Spine Systems is recalling 195 units of Calix T PEEK Lumbar System TLIF Rasps because the tools may detach and become lodged in the surgical site.
Product
Calix T PEEK Lumbar System, TLIF Rasp
Category
Medical Device
Distribution
19 states
SevereFDA (Devices)·Z-0263-2017·2016-10-26
Windstone Medical Recalls Plastic Packs with Defective Gloves
Windstone Medical Packaging is recalling 204 plastic packs used in general surgery because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Plastic Pack , Kit number AMS1833(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0124-2017·2016-10-26
Kabobs Recalls Mini Cheese Quiche Due to E. coli O121 Contamination
Kabobs Inc is recalling 377 cases of Mini Cheese Quiche because the flour used was contaminated with E. coli O121. The product was distributed across 28 states.
Product
MINI CHEESE QUICHE, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states
SevereFDA (Devices)·Z-0253-2017·2016-10-26
Windstone Medical Recalls Ortho Kits Due to Potential Sterility Compromise
Windstone Medical Packaging is recalling 145 Ortho Kits because the disposable gloves included may contain splits or holes that compromise sterility.
Product
Ortho Kit, Kit number PSS1039(A and PSS1039(B convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0134-2017·2016-10-26
Kabobs Four Cheese Puff Recalled Due to E. coli O121 Contamination
Kabobs Inc is recalling Four Cheese Puff products because they were manufactured with flour contaminated with E. coli O121.
Product
FOUR CHEESE PUFF, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0285-2017·2016-10-26
Windstone Medical Recalls Dr. Fritsch Surgical Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 224 Dr. Fritsch surgical kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Dr. Fritsch Pack, Kit number AMS2696 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0147-2017·2016-10-26
Windstone Medical Recalls Basic Surgery Kits Due to Sterility Compromise
Windstone Medical Packaging is recalling 6,381 Basic Pack surgery kits because Medtronic gloves inside may have splits or holes that compromise sterility.
Product
Basic Pack, Kit part numbers AMS1388(A, AMS1520, AMS1868, AMS1868(A, AMS1868(B, AMS2608, AMS2608(A, AMS2728, AMS2728(A, AMS2758, AMS2758(A, AMS2972, AMS4264, AMS4309, PSS1833, and PSS1848(A. convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0296-2017·2016-10-26
Ethicon Endo-Surgery Recalls Endoscopic Articulating Linear Cutters
Ethicon Endo-Surgery Inc is recalling 213 Endoscopic Articulating Linear Cutters because a pinion gear failure could interrupt the firing stroke and expose healthcare professionals to sharps injuries.
Product
Endoscopic Articulating Linear Cutter, 38ATW35. VASCULAR/THIN 35MM The ENDOPATH ETS-Flex Endoscopic Articulating Linear Cutter has application in general, gynecologic, urologic, and thoracic surgery for transection, resection, and/or creation of anastomoses
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-0191-2017·2016-10-26
Windstone Medical Recalls Foot Pack Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 85 Foot Pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Foot Pack, Kit number AMS3637 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0190-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.
Product
Facial Tray, Kit number PSS1558(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0272-2017·2016-10-26
Windstone Medical Packaging Recalls Student Pack-NS Surgical Kits
Windstone Medical Packaging is recalling Student Pack-NS surgical kits because the Medtronic gloves included may have splits or holes that compromise sterility.
Product
Student Pack-NS, Kit number PSS2788 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0194-2017·2016-10-26
Windstone Medical Recalls General Surgery Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,596 General Pack I surgery kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
General Pack I, Kit number CMP1811(B convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0228-2017·2016-10-26
Windstone Medical Recalls Lower Extremity Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 582 Lower Extremity Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Lower Extremity Pack, Kit number AMS1375(A, AMS2540, AMS2540(A, and AMS4669. convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0143-2017·2016-10-26
Kabobs Mini Vegetable Eggrolls Recalled for E. coli O121 Contamination
Kabobs Inc is recalling Mini Vegetable Eggrolls because they were made with flour contaminated with E. coli O121.
Product
MINI VEGETABLE EGGROLL, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0189-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Sterility Compromise in Surgical Kits
The FDA is recalling Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES found in Windstone Medical Packaging facial plastic kits because the gloves may contain splits or holes that compromise sterility.
Product
Facial Plastic Pack, Kit numbers AMS2533, AMS2533(A, and AMS3327 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0135-2017·2016-10-26
Kabobs Wild Mushroom in Phyllo Recalled Due to E. coli O121 Contamination
Kabobs Inc is recalling Wild Mushroom in Phyllo because it was made with flour contaminated with E. coli O121.
Product
WILD MUSHROOM IN PHYLLO, 100 CT and 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states