State

Louisiana product recalls

73,734 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,965
Critical: 1,107
Severe: 1,739
Most recent: 2026-10-28

Of the 6,965 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 1,739 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31376–31400 of 80699

ModerateFDA (Devices)·Z-2189-2020·2020-06-10
Osteomed Recalls Osteovation RMX Injectable Bone Void Filler Kits
Osteomed is recalling 278 units of Osteovation RMX Injectable Bone Void Filler kits due to incorrect shelf-life labeling that may affect product setting characteristics.
Product
OSTEOVATION RMX Injectable BVF 5CC . REF/UDI: 390-6001/ /00813845021082 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1289-2020·2020-06-10
AvKARE Recalls Lamotrigine Tablets Due to Foreign Substance Presence
AvKARE Inc. is recalling 4,124 bottles of Lamotrigine 150 mg tablets because they contain foreign substance consistent with desiccant pack granules.
Product
LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2200-2020·2020-06-10
Inpeco Aptio Automation System Recall for Firmware Error Recovery Defect
Inpeco S.A. is recalling 61 Aptio Automation Systems because a firmware error recovery procedure may dilute primary sample tubes with distilled water.
Product
Aptio Automation System using the Aliquoter Module (Inpeco P/N FLX-212) - Product Usage: The systems consolidate multiple Analytical instruments into a unified workstation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2190-2020·2020-06-10
Osteomed Recalls Osteovation Bone Void Filler Kits Due to Shelf-Life Error
Osteomed, LLC is recalling Osteovation 10 CC Impact Formula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2201-2020·2020-06-10
Trividia True Metrix Air Blood Glucose Meter Recall for Unit Error
One True Metrix Air blood glucose meter is being recalled because it displays results in mmol/L instead of mg/dL.
Product
TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip or forearm.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1288-2020·2020-06-10
Harvard Drug Group Recalls Doxycycline Hyclate Tablets for Dissolution Failure
The Harvard Drug Group is recalling Doxycycline Hyclate tablets because they failed a dissolution test at the end of their shelf life.
Product
DOXYCYCLINE HYCLATE — DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2187-2020·2020-06-10
Osteomed Recalls Osteovation 3CC ImpactFormula Bone Void Filler Kits
Osteomed is recalling 409 units of Osteovation 3CC ImpactFormula bone void filler kits due to incorrect shelf-life labeling that may affect product setting characteristics.
Product
OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2250-2020·2020-06-10
Nobel Biocare Recalls Dental Implant Healing Abutments Due to Sizing Error
Nobel Biocare is recalling specific dental implant healing abutments because they were packaged with the wrong size device.
Product
Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function. The Healing Abutment is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2184-2020·2020-06-10
Osteomed Recalls Osteovation Bone Void Filler Due to Shelf-Life Error
Osteomed is recalling 436 units of Osteovation 10cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1284-2020·2020-06-10
Triova Recalls Estriol USP Micronized 5 G Due to Impurities
Triova Pharmaceuticals is recalling Estriol USP Micronized 5 G because the product failed specifications for organic impurities.
Product
Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1286-2020·2020-06-10
Teva Recalls Mixed Amphetamine Salts Tablets Due to Strength Variations
Teva Pharmaceuticals is recalling 41,348 bottles of 15 mg Mixed Amphetamine Salts tablets because some bottles may contain mixed strengths.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2245-2020·2020-06-10
Philips Chest Pneumograph Recalled for Missing Natural Rubber Latex Labeling
Philips is recalling 1,075 Chest Pneumograph units because the labeling fails to state that the product contains natural rubber latex.
Product
Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2181-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling Osteovationex 3cc Inject Formula bone void fillers because the product may not maintain its setting characteristics for the labeled shelf-life duration.
Product
OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2169-2020·2020-06-10
FDA Recalls Sterile Custom Surgical Packs from Unregistered Facility
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.
Product
Sterile Custom Packs to be used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2208-2020·2020-06-10
Bard Equistream XK Hemodialysis Catheter Recalled for Incorrect Sheath
Bard Peripheral Vascular Inc is recalling 215 Equistream XK Long-Term Hemodialysis Catheters because the kits contain an incorrect peel-apart introducer sheath.
Product
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Category
Medical Device
Distribution
24 states
ModerateFDA (Devices)·Z-2182-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling 647 units of Osteovationex 5cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2185-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed is recalling 300 units of Osteovationex 5cc ImpactFormula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2178-2020·2020-06-10
FDA Recalls Sterile Custom Surgical Packs Due to Unregistered Facility
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.
Product
Sterile Custom Packs to be used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2249-2020·2020-06-10
Radiometer safeCLINITUBES Blood Samplers Recalled for Insufficient Aspiration
Radiometer Medical ApS is recalling safeCLINITUBES Blood Samplers because they may have insufficient aspiration capabilities, resulting in lost samples.
Product
safeCLINITUBES Blood Sampler;REF 942-969;D957P-70-45x1
Category
Medical Device
Distribution
38 states
ModerateFDA (Devices)·Z-2180-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling 70 units of Osteovationex 2cc Inject Formula because the product may not maintain its setting characteristics for the labeled shelf-life duration.
Product
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2251-2020·2020-06-10
Abbott Accelerator APS Aliquoter Module Recalled for Sample Dilution Risk
Abbott is recalling 11 Accelerator APS Aliquoter Modules because a clot detection error may cause distilled water to dilute samples, leading to incorrect clinical results.
Product
Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V340000·2020-06-09
Mercedes-Benz Metris Recall for Driveshaft Attachment Defect
Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vans because the driveshaft may not be attached correctly, risking loss of drive or unexpected airbag deployment.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V337000·2020-06-09
Jayco Recalls 2020 Motorized RVs Due to Window Glass Detachment Risk
Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.
Product
JAYCO — JAYCO, ENTEGRA REDHAWK, QWEST, SENECA, EMBLEM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V335000·2020-06-09
ARBOC Spirit of America and Liberty Buses Recalled for Fire Risk
ARBOC is recalling 113 Spirit of America and Spirit of Liberty buses because misrouted power cables may short circuit, increasing the risk of a fire.
Product
ARBOC — ARBOC SPIRIT OF AMERICA, SPIRIT OF LIBERTY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V334000·2020-06-09
Chrysler Recalls 2017-2020 Pacifica Plug-in Hybrids for Fire Risk
Chrysler is recalling 2017-2020 Pacifica Plug-in Hybrids because a high-resistance electrical connection may overheat and cause a fire.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide