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.

49951–49975 of 80793

ModerateFDA (Devices)·Z-0724-2017·2016-12-14
Halyard C-Section Drapes Recalled for Manufacturing Variation
Halyard Health is recalling specific lots of C-Section drapes because a manufacturing variation may prevent the removal of coated release paper, inhibiting easy access to the surgical site.
Product
Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with Clear Screen and Full Incise (Sterile), Product Code 44966 00; C-Section Drape with Clear Screen (Non-Sterile), Product Code 44967 NS; C-Section Drape with Clear…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0714-2017·2016-12-14
Angiodynamics Recalls PICC Catheters Due to Stylet Diameter Labeling Error
Angiodynamics Inc. is recalling specific PICC catheters because the stylet diameter may differ from the label, potentially causing stiffening.
Product
Peripherally Inserted Central Catheters (PICC), UPN H965750141, Catalog # 75-014 The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The BioFlo PICC with ENDEXO Technology and BioFlo PICC with ENDEXO and PASV Valve…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0716-2017·2016-12-14
Sorin Perceval Sutureless Aortic Heart Valve Field Action
Sorin Group USA is conducting a voluntary field action for Perceval Sutureless Aortic Heart Valves due to updated implantation procedure steps.
Product
Perceval Sutureless Aortic Heart Valve size S, Item # ICV1208, REF PVS21; Perceval Sutureless Aortic Heart Valve size M, Item # ICV1209, REF PVS23; Perceval Sutureless Aortic Heart Valve size L, Item # ICV1210, REF PVS25; Perceval Sutureless Aortic Heart Valve size XL, Item #…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0712-2017·2016-12-14
DeRoyal Recalls PneuGel Tennis Elbow Supports Due to Mold Complaints
DeRoyal Industries is recalling 56 units of PneuGel tennis elbow supports because of complaints regarding mold on the straps.
Product
TENNIS ELBOW SUPPORT, PneuGel(TM), UNIVERSAL, REF 200A10, QTY: 1 Each, Rx Only, Product Usage: Lateral and medial epicondylitis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0709-2017·2016-12-14
BioFlo PICC Nursing Kits Recalled for Incorrect Glove Expiration Dates
Navilyst is recalling BioFlo PICC Maximal Barrier Nursing Kits because the included sterile gloves have incorrect expiration dates.
Product
BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - 1) UPN # H965750121/Catalog No: 5018265, 2) UPN # H965750131/Catalog No:5024787, 3) UPN # H965750141/Catalog No: 5024787, 4) UPN # H965750241/Catalog No: 5020644, 5) UPN # H965750325/Catalog No: 5026458, 6) UPN #…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0705-2017·2016-12-14
Philips IQon Spectral CT Software Defect Recall
Philips is recalling 24 IQon Spectral CT systems due to a software defect that causes issues with filming, saving, and annotating images.
Product
IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-0717-2017·2016-12-14
Ivoclar Vivadent Recalls Virtual XD Dental Impression Material
Ivoclar Vivadent is recalling Virtual XD Refill Light Body Fast Set Wash Material because the dental impression material may fail to set up properly.
Product
Virtual XD Refill Light Body Fast Set Wash Material, 2X50 ml, REF #/Product Code 646461, Rx ONLY -- product Usage: Dental impression material
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0710-2017·2016-12-14
BioFlo PICC Nursing Kits Recalled for Incorrect Glove Expiration Dates
Angiodynamics is recalling BioFlo PICC Maximal Barrier Nursing Kits because included sterile gloves have incorrect expiration dates.
Product
BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Nursing Kit - UPN # H965750191/Catalog No:75-019 The BioFlo PICCs with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system for intravenous therapy…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0715-2017·2016-12-14
Angiodynamics Recalls PICC Catheters Due to Stylet Diameter Labeling Error
Angiodynamics is recalling PICC catheters because the stylet diameter may be larger than stated on the label.
Product
Peripherally Inserted Central Catheters (PICC), UPN H965750191, Catalog # 75-019 The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The BioFlo PICC with ENDEXO Technology and BioFlo PICC with ENDEXO and PASV Valve…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0704-2017·2016-12-14
Ultradent Recalls UltraSeal XT Plus Clear Refill Due to Labeling Error
Ultradent Products, Inc. is recalling 31 units of UltraSeal XT Plus Clear Refill, Lot BD79T, because the package was mislabeled with an incorrect part number.
Product
UltraSeal XT Plus Clear Refill. The package contains 4x 1.2 ml UltraSeal XT Plus. Product Usage: The UltraSeal XT Plus is used for prophylactic sealing of pits and fissures. It may also be used for micro restorative or initial layer of composite restorations.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0692-2017·2016-12-14
Siemens Recalls SOMATOM Force CT Systems for Software Bugs
Siemens is recalling 48 SOMATOM Force CT systems to install a software update that fixes bugs causing image errors and scan aborts.
Product
SOMATOM Force, System x-ray, tomography, computed
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0726-2017·2016-12-14
Merge PACS software recall for horizontal image cut lines
Merge Healthcare is recalling Merge PACS software because image cut lines may appear horizontally instead of vertically.
Product
Merge PACS software. Merge PACS (Picture Archiving Communication System) is designed and marketed for soft copy reading, communication and storage of studies produced by digital modalities, including digital mammography.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0718-2017·2016-12-14
Ivoclar Vivadent Recalls Virtual XD Dental Impression Material Due to Setting Failures
Ivoclar Vivadent is recalling Virtual XD Refill Light Body dental impression material because it may fail to set properly as it ages.
Product
Virtual XD Refill Light Body Regular Set Wash Material, 2X50 ml, REF #/Product Code 646462, Rx ONLY -- Product Usage: Dental impression material
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0725-2017·2016-12-14
Randox Magnesium IVD Reagent Recalled for Carryover Interference
Randox Laboratories is recalling 15 units of Magnesium IVD reagents for the RX Imola analyser due to carryover interference from amylase tests.
Product
Magnesium on RX Imola analyser IVD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0700-2017·2016-12-14
Medtronic Recalls Model 37751 Recharger for Spinal Cord Stimulation
Medtronic is recalling Model 37751 Rechargers used for spinal cord stimulation because they may become unresponsive with a blank display and beeping sound.
Product
Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is a hand-held device used to charge the battery in a patient s neurostimulator. It includes a display to provide information on the charging system. The charging system consists of the Model 37751 Recharger…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0713-2017·2016-12-14
DeRoyal Recalls Pneugel Tennis Elbow Straps Due to Mold Complaints
DeRoyal Industries is recalling 791 units of Pneugel Tennis Elbow Straps because of complaints regarding mold on the product.
Product
PNEUGEL(R) TENNIS ELBOW STRAP, UNIVERSAL, REF 12840000, QTY: 1 Each, Rx Only, Product Usage: Lateral and medial epicondylitis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0719-2017·2016-12-14
Ivoclar Vivadent Recalls Virtual XD Dental Impression Material Due to Setting Failures
Ivoclar Vivadent is recalling Virtual XD Test Pack dental impression material because it may fail to set properly as it ages.
Product
Virtual XD Test Pack Heavy/Light Fast Set, 2 x 50 ml, REF #/Product Code 646469, Rx ONLY -- Product Usage: Dental impression material
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0711-2017·2016-12-14
Encore Medical Recalls Mislabeled Empowr Knee Baseplate Implants
Encore Medical is recalling seven Empowr Knee System baseplates that were mislabeled as size 6 but are actually size 4.
Product
Empowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, utilized in either posterior cruciate ligament (PCL) retaining or PCL substituting total knee arthroplasty procedure.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0695-2017·2016-12-14
Philips Ingenuity Core CT Systems Recalled for Software Error
Philips Medical Systems is recalling 337 Ingenuity Core CT systems worldwide due to a software error involving the filament on timer.
Product
Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient…
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-0694-2017·2016-12-14
Philips Brilliance 64 CT Systems Recalled for Software Error
Philips Medical Systems is recalling 18 Brilliance 64 CT systems due to a software error involving the filament on timer.
Product
Brilliance 64 728232 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and…
Category
Medical Device
Distribution
46 states
LowFDA (Drugs)·D-0171-2017·2016-12-14
Teva Recalls Qnasl Nasal Aerosol Due to Content Uniformity Failure
Teva Pharmaceuticals USA is recalling Qnasl nasal aerosol because stability testing showed the product failed content uniformity specifications.
Product
Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg, 50 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-210-13.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0170-2017·2016-12-14
Teva Recalls Qnasl Nasal Aerosol Due to Content Uniformity Failure
Teva Pharmaceuticals is recalling Qnasl nasal aerosol canisters because the product failed stability testing for spray content uniformity.
Product
Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg, 60 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-206-06 and 59310-206-08 (Physician Samples).
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0172-2017·2016-12-14
West-Ward Recalls Sodium Ferric Gluconate Injection Due to Low Iron Content
West-Ward Pharmaceuticals is recalling 5,142 shelf-packs of Sodium Ferric Gluconate Complex in Sucrose Injection because stability testing revealed the product had lower iron content than specified.
Product
SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE — SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE (SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·F-0606-2017·2016-12-14
Safecor Vitamin B-1 Tablets Recalled for Incorrect Ingredient Labeling
Safecor Health is recalling Vitamin B-1 tablets because the boxes are labeled with the wrong chemical form of thiamine.
Product
Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed by: SAFECOR HEALTH, 317 NEW BOSTON STREET, WOBURN, MA
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·17050·2016-12-13
Cuisinart Food Processors Recalled by Conair Due to Laceration Hazard
Conair is recalling Cuisinart food processors because riveted blades can crack, posing a laceration hazard. Consumers should stop using the blades and contact Cuisinart for a free replacement.
Product
Cuisinart® food processors
Category
Consumer Product
Distribution
Distributed nationwide