State

Louisiana product recalls

72,907 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,922
Critical: 1,094
Severe: 1,483
Most recent: 2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1451–1475 of 79829

SevereFDA (Devices)·Z-2250-2026·2026-06-10
BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2026·2026-06-10
BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0910-2026·2026-06-10
Cold prep cream sauce contains dry milk recalled for Salmonella
Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2254-2026·2026-06-10
BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0909-2026·2026-06-10
Alfredo sauce contains dry milk powder recalled over Salmonella
Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2255-2026·2026-06-10
BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine
BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2256-2026·2026-06-10
BD spinal trays recalled as a sub-recall of Huons bupivacaine
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2276-2026·2026-06-10
B. Braun spinal needle kits recalled over Huons bupivacaine quality issues
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Product
Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2251-2026·2026-06-10
BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2248-2026·2026-06-10
BD Quincke spinal trays recalled over Huons bupivacaine quality issues
BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0908-2026·2026-06-10
Aramark cheese sauce contains dry milk powder recalled over Salmonella
Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Category
Food
Distribution
41 states
HighFDA (Food)·H-0980-2026·2026-06-10
Albertsons banana nut muffins do not declare walnut allergen
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Product
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2309-2026·2026-06-10
Sharpoint microsurgical knives labeled 2.2mm actually measure 3.0mm
Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.
Product
Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2026·2026-06-10
Digital angiography and radiography systems may remain energized when switched off
Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.
Product
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2026·2026-06-10
BD Pyxis MedBank Mini fingerprint scanner may overheat and burn
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1035-2026·2026-06-10
Albertsons large spring salad does not declare almond allergen
Albertsons store-made Kitchen Salad Spring Large is being recalled because the contains statement does not declare almond. 25 units are affected.
Product
UPC 29787500000 KITCHEN SALAD SPRING LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0988-2026·2026-06-10
Albertsons 16-inch carving tray does not declare walnut
An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.
Product
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0961-2026·2026-06-10
Cakerie strawberry shortcake triangles do not declare hazelnut allergen
Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.
Product
UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0557-2026·2026-06-10
Kirkland Signature ultra strength antacid tablets contain metallic particles
Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.
Product
KIRKLAND ULTRA STREGTH ANTACID 171AB — KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1020-2026·2026-06-10
Albertsons chicken strip salad does not declare almond allergen
Albertsons store-made Kitchen Salad Chicken Strip is being recalled because the contains statement does not declare almond. 55 units are affected.
Product
UPC 29433900000 Kitchen SALAD CHICKEN STRIP This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2286-2026·2026-06-10
Philips Azurion 5M12 systems may show unusable dark fluoroscopy images
Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.
Product
Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1073-2026·2026-06-10
Albertsons berry and salmon salad omits salmon and walnut declarations
Albertsons store-made Fresh Berry & Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. 90 units are affected.
Product
UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1022-2026·2026-06-10
Albertsons fresh berry and chicken salad does not declare walnut
Albertsons store-made Ready Meals Salad Fresh Berry & Chicken is being recalled because the contains statement does not declare walnut. 228 units are affected.
Product
UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2275-2026·2026-06-10
PhaseOne antimicrobial solution sprayer springs may corrode into the product
PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1026-2026·2026-06-10
Albertsons Cheeses of France platter does not declare almond
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
Product
UPC 27837800000 PLATTER CHEESES OF FRANCE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide