State

Louisiana product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34401–34425 of 80703

HighFDA (Devices)·Z-0293-2020·2019-11-13
Argon Medical Devices Recalls Vascuclamp Vascular Clamps Due to Sterility Risk
Argon Medical Devices is recalling Vascuclamp radiopaque vascular clamps because an incomplete pouch seal may cause a loss of sterility.
Product
(1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-1-200, 2 clamps/package, 5 packages/box, 10 boxes/case, Sterile, Rx; (2) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Medium Straight, REF 046-1-300, 2 clamps per package…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0289-2020·2019-11-13
Argon Medical Devices Recalls Double Male LL Adapter Due to Seal Defect
Argon Medical Devices is recalling Double Male LL Adapters because an incomplete pouch seal may cause a loss of sterility.
Product
Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0338-2020·2019-11-13
Zimmer Biomet Recalls Cable Buttons for Polyaxial Locking Plates
Zimmer Biomet is recalling cable buttons for NCB Polyaxial Locking Plates because non-highly polished implants may adhere to the packaging bag.
Product
cable button for NCB¿ Polyaxial Locking Plate, 2.5 mm Hex Drive, Item No. 47223206001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0269-2020·2019-11-13
Ortho-Clinical Diagnostics Recalls VITROS K+ Slides Due to Dispense Issues
Ortho-Clinical Diagnostics is recalling VITROS K+ Slides because a mechanical failure may cause intermittent slide dispense issues.
Product
VITROS chemistry Products K+ Slides, Catalog No. 8157596. MicroSlides which contain reagents in a dry, multi-layered form.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0340-2020·2019-11-13
Western / Scott Fetzer Recalls Grab n Go Opti VIPR Oxygen Systems
Western / Scott Fetzer is recalling 143,164 Grab n Go Opti VIPR oxygen systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Product
Grab n Go Opti series VIPR system Model # PRX-9627 - Product Usage: The Grab n Go Opti system is an integrated delivery system intended to provide supplemental oxygen, by Rx only, to patients. When administered by properly trained personnel for oxygen deficiency and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0307-2020·2019-11-13
Zimmer Biomet Recalls Tibial Plates Due to Packaging Adhesion
Zimmer Biomet is recalling 5.4 million tibial plates because non-highly polished implants may adhere to the packaging bag.
Product
Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 00234700312 00234700314 00234700316 00234700404 00234700406 00234700408 00234700410 00234700412 00234700414 00234700416 00234700502 00234700504 00234700506 00234700508…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0268-2020·2019-11-13
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Cl- Slides Due to Dispense Issues
Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because the anti-backup platen may fail to advance, causing intermittent slide dispense issues.
Product
VITROS chemistry Products Cl- Slides, Catalog No. 8445207 (which does NOT support Urine CL-). MicroSlides which contain reagents in a dry, multi-layered form.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0336-2020·2019-11-13
Zimmer Biomet Recalls Ceramic Femoral Heads Due to Packaging Adhesion
Zimmer Biomet is recalling 5.4 million ceramic femoral heads because non-highly polished implants may adhere to the LDPE bag packaging.
Product
Ceramic Femoral Heads, various sizes, Item Nos. 00877504001 00877504002 00877504003 00877504004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0270-2020·2019-11-13
Pega Medical Recalls SCFE Knobs for Driver Due to Screw Loosening Risk
Pega Medical Inc. is recalling 31 SCFE Knobs for Driver because screws may loosen during ultrasonic cleaning and fall out.
Product
SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0305-2020·2019-11-13
Zimmer Biomet Recalls ZPLP Fibular Plates Due to Packaging Adhesion
Zimmer Biomet is recalling ZPLP Fibular Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Product
ZPLP Fibular Plate, Item Nos. 00234701504 00234701506 00234701508 00234701510 00234701512 00234701516 00234701604 00234701606 00234701608 00234701610 00234701612 00234701614 00234701616 00234701702 00234701704 00234701706 00234701708 00234701710 00234701712…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0304-2020·2019-11-13
Zimmer Biomet Recalls NCB Periprosthetic Proximal Femoral Plates
Zimmer Biomet is recalling NCB Periprosthetic Proximal Femoral Plates because non-highly polished implants may adhere to the packaging bag.
Product
NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 0202263015 0202263018 0202263021 0202263109 0202263112 0202263115 0202263118 0202263121 0202264009 0202264012 0202264015 0202264018 0202264021 0202264109 0202264112…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0319-2020·2019-11-13
Zimmer Biomet Recalls CLS Brevius Stem Kinectiv Hip Prostheses
Zimmer Biomet is recalling CLS Brevius Stem Kinectiv hip prostheses because non-highly polished implants may adhere to the packaging bag.
Product
CLS Brevius Stem Kinectiv, hip prosthesis, various sizes. Item Nos. 0100296050 0100296060 0100296070 0100296080 0100296090 0100296100 0100296112 0100296125 0100296137 0100296150 0100296162 0100296175 0100296200
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0282-2020·2019-11-13
Randox Rheumatoid Factor Standard Recalled for Value Adjustment
Randox Laboratories is recalling 17 Rheumatoid Factor Standard kits because assigned values over-recovered against reference material. The values have been adjusted to align with the reference standard.
Product
Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN: 05055273205039 Product Usage: The Randox Rheumatoid Factor Latex-Enhanced Immunorutbidimetric Test Kit is an in vitro diagnostic reagent for the quantitative determination of rheumatoid factors (RF) in human…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0328-2020·2019-11-13
Zimmer Biomet Recalls Various Fixation Systems and Accessories
Zimmer Biomet is recalling various fixation systems and accessories because non-highly polished implants may adhere to the LDPE bag.
Product
Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924 00224000926 00224000928 00224000930 00224000932 00224000934 00224000936 00224000938 00224000940 00224000942 00224000944 00224000946 00224001014…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0312-2020·2019-11-13
Zimmer Biomet Recalls Universal Locking Plates Due to Packaging Adhesion
Zimmer Biomet is recalling 5.4 million Universal Locking Plates because non-highly polished implants may adhere to the packaging bag.
Product
Universal Locking Plates Sterile, Item Nos. 47492800207 47492800303 47492800402 47492800403 47492800407 47492800502 47492800503 47492800507 47492800603 47492800607 47492800613 47492800702 47492800703 47492800707 47492800802 47492800803 47492800807 47492800813…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0314-2020·2019-11-13
Zimmer Biomet Recalls Periarticular Elbow and Humeral Plates
Zimmer Biomet is recalling specific periarticular plates because non-highly polished implants may adhere to the packaging bag.
Product
Periarticulare Plates - Elbow, Humeral and Ulna Plates, Item Nos. 00234800504 00234800506 00234800508 00234800510 00234800512 00234800514 00234800604 00234800606 00234800608 00234800610 00234800612 00234800614 00234800712 00234800714 00234800716 00234800902…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0310-2020·2019-11-13
Zimmer Biomet Recalls Distal Lateral Femoral Locking Plates
Zimmer Biomet is recalling 5,459,583 sterile distal lateral femoral locking plates because non-highly polished implants may adhere to the packaging bag.
Product
DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 47235710122 47235710210 47235710214 47235710218 47235710222
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0286-2020·2019-11-13
Biomedical Polymers Recalls Hemo-Drop Blood Dispensers Due to Metal Cannula Defect
Biomedical Polymers, Inc. is recalling 108,000 Hemo-Drop Blood Dispensers because the metal cannula may break or fail to pierce the specimen tube.
Product
Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0263-2020·2019-11-13
FDA Recalls Autoject EI Medical Devices Due to Possible Assembly Error
Owen Mumford USA is recalling 1,510 units of Autoject EI devices due to a possible assembly error. The lot was distributed to 13 states.
Product
Autoject EI, REF AJ1310
Category
Medical Device
Distribution
13 states
ModerateFDA (Devices)·Z-0315-2020·2019-11-13
Zimmer Biomet Recalls Peri Dist Volar/Dorsal T/Dorsal Delta Radial Implants
Zimmer Biomet is recalling specific wrist implants because non-highly polished devices may adhere to the packaging bag.
Product
PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 00234801308 00234801310 00234801312 00234801403 00234801404 00234801406 00234801408 00234801410 00234801412 00234802102 00234802104 00234802106 00234802108 00234802110…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0320-2020·2019-11-13
Zimmer Biomet Recalls Fitmore Hip Stems Due to Packaging Adhesion
Zimmer Biomet is recalling Fitmore Hip Stems because non-highly polished implants may adhere to the LDPE bag used in previous packaging configurations.
Product
Fitmore Hip Stem, hip prosthesis, various sizes, Item Nos. 0100551102 0100551103 0100551104 0100551105 0100551106 0100551107 0100551108 0100551109 0100551110 0100551111 0100551112 0100551113 0100551114 0100551201 0100551202 0100551203 0100551204 0100551205…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0331-2020·2019-11-13
Zimmer Biomet Recalls NCB Straight Narrow Plates Due to Packaging Adhesion
Zimmer Biomet is recalling NCB Straight Narrow Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Product
NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008 0202267010 0202267012 0202267014 0202267016 0202267018
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0309-2020·2019-11-13
Zimmer Biomet Recalls Tibia Lock Plates Due to Packaging Adhesion
Zimmer Biomet is recalling Prox Lat Tib Lock Plates and Dist Med Tib Lock Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Product
Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 47235700314 47235700408 47235700410 47235700412 47235700414 47235700416 47235700504 47235700506 47235700508 47235700510 47235700512 47235700514…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0324-2020·2019-11-13
Zimmer Biomet Recalls LPS-MOB Articular Surface Implants Due to Packaging Issue
Zimmer Biomet is recalling 5,459,583 LPS-MOB Articular Surface Implants because non-highly polished implants may adhere to the LDPE bag.
Product
LPS-MOB ART SURF IMPL D 9MM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0317-2020·2019-11-13
Zimmer Biomet Recalls Periarticular Locking Elbow Plates Due to Packaging Adhesion
Zimmer Biomet is recalling 5.4 million periarticular locking elbow plates because non-highly polished implants may adhere to the packaging bag.
Product
Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 47235800603 47235800605 47235800607 47235800609 47235800611 47235800615 47235800619 47235800705 47235800711 47235800715 47235800803 47235800805…
Category
Medical Device
Distribution
Distributed nationwide