State

Louisiana product recalls

73,570 recalls have nationwide distribution and so reach Louisiana. 6,960 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,960
Critical: 1,109
Severe: 1,737
Most recent: 2026-10-21

Of the 6,960 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 1,737 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,960 recalls whose distribution notice names Louisiana specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26401–26425 of 80530

HighFDA (Devices)·Z-2131-2021·2021-07-28
Exactech Hip Implant Liners Recalled Due to Premature Wear Risk
Exactech is recalling certain acetabular polyethylene hip implant liners due to risk of edge-loading and premature wear in specific implant configurations and surgical positions.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 138-28-XX, Acumatch GXL 15 Degree, +5 Lat Liner, 28mm; Novation GXL 10 Deg Liner, G0, 28mm; and Novation GXL Liner, 10 Deg Face, 28mm. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V577000·2021-07-28
2022 Kia Telluride Instrument Cluster Display May Go Blank
Certain 2022 Kia Telluride vehicles have instrument cluster displays that may go blank after startup, potentially hiding critical driving information like speed and gear selection. Kia will update the software at no cost.
Product
KIA — KIA TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2092-2021·2021-07-28
Blood heater-cooler devices recalled for water contamination and infection risk
Gentherm's Hemotherm CE blood cooler/heater devices may harbor dangerous organisms including nontuberculous mycobacteria in their water systems that could aerosolize during cardiac surgery, risking patient infection.
Product
Hemotherm CE Dual Reservoir Cooler/Heater, Model 400CE, 115V Model, part no. 86022. Used to cool or warm blood during cardiopulmonary bypass procedures
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V575000·2021-07-28
Forest River Recalls 2021 Prime Time Tracer Trailers Due to Tail Light Defect
Forest River is recalling 2021 Prime Time Tracer TRT22RBS recreational trailers because the tail light is located too close to the water heater exhaust, which may cause the light to fail.
Product
PRIME TIME — PRIME TIME TRACER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2104-2021·2021-07-28
DJO Surgical EMPOWR 3D Knee Tibial Insert packaging may contain wrong implant size
Packaging for DJO Surgical EMPOWR 3D Knee Tibial Insert knee prosthesis implants may be mislabeled, with 12mm packages potentially containing 16mm implants or vice versa, risking incorrect surgical implantation.
Product
DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-16-711 Left Sz. 11 16mm, CE 0086, Sterile H2O2, UDI: (01)00888912167185
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2112-2021·2021-07-28
Exactech Connexion GXL Hip Implant Liners Recalled for Premature Wear Risk
Exactech Connexion GXL hip implant liners are being recalled due to risk of edge-loading and premature wear in certain surgical configurations. Approximately 89,050 units distributed nationwide may be affected.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 104-28-XX, MCS +5GXL Liner 5/15 DEG and MCS GXL Liner 5/15 DEG. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2125-2021·2021-07-28
Exactech Connexion GXL hip implant liners recalled for premature wear risk
Exactech is recalling 89,050 hip implant liners due to edge-loading and premature wear risk in a subset of patients with certain implant configurations.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 136-22-XX, Novation GXL Liner, +5mm Lateralized, G00, 22mm ID. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2127-2021·2021-07-28
Exactech Connexion GXL Hip Implant Liners Recall Risk of Premature Wear
Exactech is recalling 89,050 Connexion GXL acetabular hip implant liners due to risk of edge-loading and premature wear in certain patient configurations and surgical placements.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 136-32-XX, Novation GXL Liner, +5mm Lateralized, 32mm. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2120-2021·2021-07-28
Exactech Hip Implant Liners Recalled for Premature Wear Risk
Exactech Connexion GXL acetabular polyethylene liners used in hip implants face premature wear risk in certain patient and implant configurations. Consult your orthopedic surgeon if you have this device.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-22-XX, Novation GXL Liner, G00, 22mm ID; and Novation GXL Liner, Lipped Ant, 28mm. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2021·2021-07-28
Hip Implant Liners Recalled Due to Risk of Premature Wear
Exactech Connexion GXL hip implant liners are being recalled due to a risk of edge-loading and premature prosthesis wear in patients with certain implant configurations and surgical positioning.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-36-XX, Acumatch GXL 15 Degree Liner, 36mm, and Novation GXL Liner, Lipped Ant, 36mm; and Novation GXL Liner, Lipped, 36mm. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2114-2021·2021-07-28
Hip implant liners recalled due to risk of premature wear
Exactech is recalling 89,050 hip implant liners due to risk of edge-loading and premature wear in specific patient and surgical configurations affecting a subset of patients.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 104-36-XX, MCS +5GXL Liner 5/15 DEG and MCS GXL Liner 5/15 DEG. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2098-2021·2021-07-28
SoftCytogenetics Software Recalled for Incorrect Test Result Transmission
Soft Computer Consultants, Inc. is recalling SoftCytogenetics software (versions 4.1.11.20, 4.1.12.11, 4.1.15.6) distributed in CA, FL, MN, and NJ because it produces incorrect results for retested specimens that are transmitted to clinical information systems.
Product
SoftCytogenetics
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2094-2021·2021-07-28
Infant Heel Warmer Units Recalled for Rupture and Chemical Splashing Risk
Cardinal Health is recalling 926,425 infant heel warmers (SKU MH00002T) due to reports of pack rupture or leaking during activation. The heated liquid may splash into a user's eyes or onto an infant, potentially causing rash, burn, or inflammation.
Product
Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at the point of care by squeezing the pouch. This mixes the substrates inside the pouch causing an exothermic chemical reaction, warming the pouch, which is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2121-2021·2021-07-28
Exactech GXL Acetabular Hip Implant Liners Recalled for Premature Wear Risk
Exactech, Inc. is recalling 89,050 Connexion GXL and Novation GXL acetabular hip implant liners due to risk of edge-loading and premature prosthesis wear in certain patients. The risk depends on implant configuration and surgical positioning.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-28-XX, Acumatch GXL 15 Degree Liner, 28mm; Novation GXL Liner, G0, 28mm ID; Novation GXL Liner, Lipped Ant, 28mm; and Novation GXL Liner, Lipped, 28mm. Orthopedic hip…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2081-2021·2021-07-28
Moderna COVID-19 Vaccine Administration Kits Recalled for Unsuitable Syringes
McKesson is recalling 53,388 Moderna COVID-19 vaccine administration kits due to unsuitable 3mL syringes included in the kits. The affected kits were distributed May 4-24, 2021, and should not be used for vaccine administration.
Product
ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2101-2021·2021-07-28
Stryker Cortoss Bone Augmentation Material Recalled for Temperature Storage Violation
Stryker Spine recalled Cortoss Bone Augmentation Material due to a 12-hour temperature excursion at the distribution center that could have compromised product sterility and efficacy.
Product
Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21172·2021-07-28
Birkenstock Kids' Mogami Sandals Recalled for Choking Hazard
Birkenstock USA has recalled Kids' Mogami Sandals in sizes 24-28 because a plastic rivet can detach from the ankle strap, posing a choking hazard for young children. No injuries have been reported.
Product
Birkenstock Kids' Mogami Sandals Sizes 24-28
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2103-2021·2021-07-28
Knee Prosthesis Recall: Packaging Mixup May Cause Wrong Size Implantation
Encore Medical recalls DJO Surgical EMPOWR 3D knee prosthetic components because packaging labels may not match the product inside, risking implantation of incorrect prosthesis sizes.
Product
DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI: (01)00888912166980
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2100-2021·2021-07-28
Cortoss Bone Augmentation Material Recalled Due to Storage Temperature Excursion
Stryker Spine is recalling 559 units of Cortoss Bone Augmentation Material 5cc Cartridges due to a 12-hour temperature excursion at the distribution center. The affected lot may not meet required storage conditions.
Product
Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2021·2021-07-28
Hip implant acetabular liners recalled for edge-loading and premature wear
Exactech Connexion GXL acetabular polyethylene liners for hip implants are recalled due to risk of edge-loading and premature wear in certain patient configurations and implant positions. Approximately 89,050 units distributed nationwide are affected.
Product
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-32-XX, Acumatch GXL 15 Degree Liner, 32mm; Novation GXL Liner, Lipped Ant, 32mm; and Novation GXL Liner, Lipped, 32mm. Orthopedic hip implant component.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0689-2021·2021-07-28
Erythromycin Topical Solution 2% Recalled for Failed Impurities Specifications
Teligent Pharma, Inc. is recalling Erythromycin Topical Solution USP 2% (60 mL, Lot 14180) distributed nationwide because it failed impurities and degradation specifications.
Product
Erythromycin Topical Solution USP, 2% 60 mL, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310, NDC 52565-027-59
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2108-2021·2021-07-28
Mindray battery cradle may prevent monitor from powering on
Mindray is recalling the 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 and TM80 Telepack physiological monitors. The cradle may prevent the monitor from powering on. Approximately 804 units were distributed in the US and Canada.
Product
3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0690-2021·2021-07-28
Erythromycin Topical Gel 2% Recalled Due to Failed Impurity Specifications
Teligent Pharma, Inc. is recalling Erythromycin Topical Gel 2% due to failed impurities and degradation specifications. The recall affects approximately 22,824 tubes distributed nationwide.
Product
Erythromycin Topical Gel, 2%, Net Wt. (a) 30 g,(NDC 52565-033-30) (b) 60 g,(NDC 52565-033-60) Rx Only, Manufactured by: Teligent Pharma, Inc. , Buena, NJ 08310,
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V574000·2021-07-27
Mack Recalls 2022 MD Trucks Due to Loose Front Suspension Bolts
Mack Trucks is recalling 2022 MD trucks because loose front suspension bolts may detach, potentially causing loss of vehicle control and increasing crash risk.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V573000·2021-07-27
Mack Trucks Recalls 2021 LR, Granite, and TE Models for Brake Defect
Mack Trucks is recalling 2021 LR, Granite, and TE vehicles because incorrect rear brake cams may cause inoperative rear axle brakes, increasing crash risk.
Product
MACK — MACK LR, GRANITE (GR), TE
Category
Vehicle
Distribution
Distributed nationwide