State

Louisiana product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36551–36575 of 80706

HighFDA (Devices)·Z-1743-2019·2019-06-12
Bio-Rad Recalls MRSASelect II Diagnostic Plates Due to Abnormal Coloration
Bio-Rad Laboratories is recalling MRSASelect II diagnostic plates due to abnormal agar coloration and non-characteristic colony growth. The recall covers 3,632 units distributed nationwide.
Product
MRSASelect II, IVD, REF 63758 (20 plates per package). The MRSASelect is indicated for use in conjunction with other laboratory tests and clinical data available to aid in the identification and diagnosis of MRSA from patients with skin and soft-tissue infections.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1692-2019·2019-06-12
Philips IntelliVue MX40 Patient Monitor Recalled for Battery Defect
Philips is recalling IntelliVue MX40 Patient Monitors because they may experience increased power consumption and lack visual or audible notifications when in a low battery state.
Product
IntelliVue MX40 Patient Monitor, Product number 865350, Service # USA: 453564262491 and 453564262511 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2019·2019-06-12
Zimmer Biomet Recalls Oxford Partial Knee Drill Guides Due to Corrosion Risk
Zimmer Biomet is recalling 3 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw materials may cause corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1726-2019·2019-06-12
Stryker High Flow II Tube Set Recalled for Leaking and Detachment
Stryker is recalling High Flow II Tube Sets because they consistently leak and detach from the cassette. The product is a medical device accessory distributed nationwide and internationally.
Product
Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2019·2019-06-12
AngioDynamics Solero Microwave Tissue Ablation System Recall for Delayed Procedures
AngioDynamics is recalling 178 Solero Microwave Tissue Ablation System generators to update manuals and software, reducing the risk of patient harm from procedure delays.
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H78712740000D0 (2) Solero Generator Refurbished US PG Catalog Number: 12740000USD ;UPN: H78712740000USD0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1712-2019·2019-06-12
Flowonix Prometra Clinician Programmer Software Recall for Unexpected Pump Shutdowns
Flowonix Medical Inc is recalling Prometra Clinician Programmer software due to a defect that can cause intrathecal pumps to shut down unexpectedly.
Product
Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat. No. 12828, used with Prometra and Prometra II Programmable Pumps. For intrathecal infusion.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1737-2019·2019-06-12
Zimmer Biomet Recalls Oxford Partial Knee Drill Guides Due to Material Error
Zimmer Biomet is recalling 10 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used, potentially leading to corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1695-2019·2019-06-12
Philips IntelliVue MX40 Patient Monitor Recalled for Battery Notification Defects
Philips is recalling IntelliVue MX40 Patient Monitors because they may fail to provide visual or audible alerts when the battery is low.
Product
IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2019·2019-06-12
AngioDynamics Solero Microwave Tissue Ablation System Recall for Delayed Procedure Risk
AngioDynamics is recalling Solero Microwave Tissue Ablation System applicators to reduce the risk of patient harm from delayed procedures via manual and software updates.
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Applicator 14cm PG Catalog Number: 700106001 UPN:H7877001060010; (2)Solero Applicator 14cm PG US Catalog Number:700106001US UPN: H787700106001US0 Product Usage: The Solero Microwave Tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1693-2019·2019-06-12
Philips IntelliVue MX40 Patient Monitor Recalled for Battery Issues
Philips is recalling IntelliVue MX40 Patient Monitors because they may consume excess power and fail to provide visual or audible low-battery alerts.
Product
IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 453564467821, 453564467841, 453564467861, 453564262531, and 453564262551 - Product…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1714-2019·2019-06-12
Flowonix Prometra Programmable Pump Recalled for Unexpected Shutdowns
Flowonix Medical Inc. is recalling 809 Prometra Programmable Pumps because a software defect can cause the pump to shut down unexpectedly.
Product
Prometra Programmable Pump, Cat. No. 11827 For intrathecal infusion.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1727-2019·2019-06-12
Stryker High Flow Tube Set Recalled for Leaking and Detachment
Stryker is recalling High Flow Tube Sets with Real-Time Pressure Sensing because they consistently leak and detach from the cassette.
Product
Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-680, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2019·2019-06-12
Stryker AXS Infinity LS Plus Long Sheath Recalled for Brittle Behavior
Stryker Neurovascular is recalling AXS Infinity LS Plus Long Sheaths because a design issue can cause the device to become brittle and fracture.
Product
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO (916-3876): a) REF: INC-11196-70, 70cm, b) REF: INC-11196-80, 80cm, c) REF: INC-11196-90, 90cm Product Usage: Indications for Use: The AXS Infinity LS Plus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2019·2019-06-12
Zimmer Biomet Recalls Oxford Partial Knee Drill Guides Due to Corrosion Risk
Zimmer Biomet is recalling 14 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw materials were used, potentially leading to corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small
Category
Medical Device
Distribution
7 states
HighCPSC·19137·2019-06-12
Mares Recalls XR Buoyancy Compensation Vests Due to Drowning Hazard
Mares is recalling XR buoyancy compensation vests because the deflation button can unscrew, causing loss of buoyancy and a drowning hazard. No injuries have been reported.
Product
Mares XR buoyancy compensation vests
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2019·2019-06-12
Philips IntelliVue MX40 Patient Monitor Recalled for Battery Notification Issues
Philips is recalling IntelliVue MX40 Patient Monitors because they may fail to provide visual or audible low-battery alerts, potentially disrupting patient monitoring.
Product
IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564615351, and 453564615371 Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1728-2019·2019-06-12
Stryker Heated Tube Set Recall for Leaking and Detachment Issues
Stryker is recalling 19,083 boxes of Heated Tube Sets with Real-Time Pressure Sensing because they consistently leak and detach from the cassette.
Product
Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2019·2019-06-12
AngioDynamics Solero Microwave Tissue Ablation System Recall for Delayed Procedures
AngioDynamics is recalling 314 Solero Microwave Tissue Ablation System generators to update manuals and software, reducing the risk of patient harm from procedure delays.
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN: H78712740000 (2) Solero Generator US PG Catalog Number: 12740000US UPN: H78712740000US0 (3) Solero Generator Service Loaner PG Catalog No: 12740000L…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1704-2019·2019-06-12
AngioDynamics Solero Microwave Tissue Ablation System Recall for Procedure Delay Risk
AngioDynamics is recalling 1,846 Solero Microwave Tissue Ablation System applicators to reduce the risk of patient harm from procedure delays.
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 29cm PG Catalog Number:700106003 UPN: H7877001060030 (2)Solero Applicator 29cm PG US Catalog Number:700106003US UPN:H787700106003US0 Product Usage: The Solero Microwave Tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1719-2019·2019-06-12
Centurion Medical Recalls Sterile Nail Clippers Due to Compromised Seals
Centurion Medical Products Corporation is recalling sterile nail clippers because the sterile barrier pouch seals are compromised, potentially affecting sterility.
Product
Sterile Nail Clipper Concave Edge (67710)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2019·2019-06-12
Zimmer Biomet Recalls Oxford Partial Knee Drill Guides Due to Corrosion Risk
Zimmer Biomet is recalling 41 Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used in the screw component, which could lead to corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420321 Phase 3 Femoral Drill Guide Small
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1713-2019·2019-06-12
Flowonix Prometra Programmer Software Recall for Unexpected Pump Shutdowns
Flowonix Medical Inc is recalling 40 units of Prometra Programmer software due to a defect that causes intrathecal pumps to shut down unexpectedly.
Product
Prometra Programmer (Grand Prime) Software version 2.00.29, Cat. No. 13828, used with Prometra and Prometra II Programmable Pumps. For intrathecal infusion.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1738-2019·2019-06-12
Zimmer Biomet Recalls Oxford Partial Knee Drill Guides Due to Material Error
Zimmer Biomet is recalling 11 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used, potentially leading to corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1703-2019·2019-06-12
AngioDynamics Solero Microwave Tissue Ablation System Recall for Delayed Procedures
AngioDynamics is recalling 7,348 Solero Microwave Tissue Ablation applicators to update manuals and software, reducing the risk of patient harm from procedure delays.
Product
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 19cm PG Catalog Number: 700106002 UPN: H7877001060020 (2)Solero Applicator 19cm PG US Catalog Number:700106002US UPN: H787700106002US0 Product Usage: The Solero Microwave Tissue…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1742-2019·2019-06-12
Bio-Rad Recalls MRSASelect In Vitro Diagnostic Plates Due to Abnormal Coloration
Bio-Rad Laboratories is recalling 5,212 units of MRSASelect in vitro diagnostic plates due to abnormal agar coloration and non-characteristic colony growth.
Product
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with other laboratory tests and clinical data available to aid in the identification and diagnosis of MRSA from patients with skin and soft-tissue infections.
Category
Medical Device
Distribution
Distributed nationwide