The Recall Desk

State

Louisiana product recalls

72,968 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.

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5926–5950 of 79890

  • SevereFDA (Devices)·Z-2183-2025·2025-08-13

    BritePro Solo laryngoscope handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac 1), 040-332U (Mac 2), 040-333U (Mac 3), 040-335U (Mac 3.5) 040-334U (Mac 4), 040-341U (Miller 1), 040-342U (Miller 2), 040-343U (Miller 3), 040-344U (Miller 4), 040-361U (Phillips 1), 040-36
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2186-2025·2025-08-13

    BritePro Solo mini laryngoscope handles may not illuminate as intended

    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2187-2025·2025-08-13

    BritePro Solo fiber optic laryngoscope handles may not illuminate properly

    BritePro Solo Single-Use Fiber Optic Laryngoscope Handles, REFs 040-310AU and 040-310U, are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2185-2025·2025-08-13

    BritePro Solo stubby laryngoscope handles may not illuminate as intended

    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0419-2025·2025-08-13

    Italian layer cake recalled because its pecans may carry Salmonella

    Item #1071 Italian layer cake is being recalled because the pecans used in it have the potential to be contaminated with Salmonella. The source does not state a quantity.

    Product
    Item #1071 Italian layer cake
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0574-2025·2025-08-13

    Spironolactone 25 mg tablets recalled after aluminum was found in product

    Spironolactone Tablets USP 25 mg are being recalled because of the presence of a foreign substance identified as aluminum. 11,328 bottles are affected.

    Product
    SPIRONOLACTONE — SPIRONOLACTONE (SPIRONOLACTONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0568-2025·2025-08-13

    Direct Rx duloxetine 30 mg capsules exceed the interim nitrosamine limit

    Duloxetine Delayed-Release 30 mg capsules packaged by Direct Rx are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 875 bottles affected.

    Product
    Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle NDC 61919-0482-30, b) 60-count bottle, NDC 61919-0482-60, c) 90-count bottle, NDC 61919-0482-90; Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0383-2025·2025-08-13

    Queen Bee Gardens pure whipped honey may contain stainless steel flakes

    Queen Bee Gardens Whipped Honey Pure in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 112 jars are affected.

    Product
    Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182006. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2277-2025·2025-08-13

    Stryker SmartPump tourniquet cuff flanges may detach from the bladder

    Stryker SmartPump Tourniquet disposable cuffs are being recalled because the cuff flange may become detached from the bladder, which the manufacturer links to a risk of hemorrhage if a leak occurs during a procedure.

    Product
    Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK / 5921-018-235; DISP 24X4,1BLA, 2PRT QUICK / 5921-024-235
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0382-2025·2025-08-13

    Queen Bee Gardens raspberry whipped honey may contain stainless steel flakes

    Queen Bee Gardens Whipped Honey Raspberry in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 129 jars are affected.

    Product
    Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182358. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0566-2025·2025-08-13

    Doxepin hydrochloride capsules exceed the interim nitrosamine impurity limit

    Doxepin Hydrochloride Capsules USP 10 mg from Alembic are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 9,492 bottles affected.

    Product
    DOXEPIN HYDROCHLORIDE — DOXEPIN HYDROCHLORIDE (DOXEPIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2272-2025·2025-08-13

    epoc BUN test cards may show a negative sodium bias

    epoc BGEM BUN Test Cards are being recalled because a negative sodium bias may exist in some lots, with an observed average bias of -4.4 mmol/L. 37,554 units are affected.

    Product
    epoc BGEM BUN Test Card [25pk]. Material Number: 10736515.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0384-2025·2025-08-13

    Queen Bee Gardens whipped honey may contain stainless steel flakes

    Queen Bee Gardens Whipped Honey Huckleberry in 11 oz jars is being recalled because the product may have small flakes of stainless steel in it. 24 jars are affected.

    Product
    Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Intended use: spread. Item is shelf stable. Packaging type: Jar. Net wt., 11oz. UPC: 788394182259. Firm Name: Queen Bee Gardens Firm Address: 262 East Main Street, Lovell, WY 82431
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2239-2025·2025-08-13

    Pinnacle 3 radiation planning software may miscalculate stopping power ratio

    Pinnacle 3 with TumorLOC Radiation Therapy Planning System software is being recalled because a software issue may provide incorrect dataset calculations when performing the Stopping Power Ratio. 149 serial numbers affected.

    Product
    Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0567-2025·2025-08-13

    Duloxetine delayed-release capsules exceed the interim nitrosamine impurity limit

    Duloxetine Delayed-Release 20 mg capsules packaged by Direct Rx are being recalled because a nitrosamine drug substance related impurity was present above the proposed interim limit. 16 bottles affected.

    Product
    Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only, Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, NDC 61919-422-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0552-2025·2025-08-13

    Duloxetine 60 mg capsules exceed the safety assessment limit for nitrosamine

    Duloxetine Delayed-Release Capsules USP 60 mg distributed by Breckenridge are being recalled because N-nitroso-duloxetine was present above the safety assessment limit. 1,829 bottles affected.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0410-2025·2025-08-13

    Pillsbury cinnamon rolls recalled after a shipping trailer temperature excursion

    Pillsbury Cinnamon Rolls with Original Icing, 8 count, are being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Pillsbury Cinnamon Rolls Original Icing, 8 ct., NET WT 12.4 OZ (351g), packaged in a cardboard and aluminum tube, UPC: 018000005017
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0408-2025·2025-08-13

    Minute Maid fruit punch recalled after a shipping trailer temperature excursion

    Minute Maid Fruit Punch, 59 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 4 units are affected.

    Product
    Minute Maid Fruit Punch, 59 FL OZ (1.8 QT) 1.75 L, packaged in a paper carton, UPC: 025000047732
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0411-2025·2025-08-13

    Shamrock Farms protein shakes recalled after a shipping trailer temperature excursion

    Shamrock Farms Chocolate Rockin' Protein Builder Protein Shake, 12 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units affected.

    Product
    Shamrock Farms Chocolate Rockin' Protein Builder Protein Shake, 12 FL OZ (354 ML), packaged in a plastic bottle, UPC: 028300004054
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0413-2025·2025-08-13

    Silk vanilla almondmilk recalled after a shipping trailer temperature excursion

    Silk Vanilla AlmondMilk, 64 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Silk Vanilla AlmondMilk, 64 FL OZ (2 QT) 1.89 L, packaged in a paper carton, UPC: 025293000995
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0406-2025·2025-08-13

    Milo's extra sweet tea recalled after a shipping trailer temperature excursion

    Milo's Extra Sweet Tea, 1 gallon, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 3 units are affected.

    Product
    Milo's Extra Sweet Tea, 128 FL OZ (1 GAL) 3.78 L, packaged in a plastic jug, UPC: 091475931982
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0414-2025·2025-08-13

    Simply Orange juice recalled after a shipping trailer temperature excursion

    Simply Orange Pulp Free Orange Juice in 46 fl oz and 11.5 fl oz bottles is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 2 units affected.

    Product
    1) Simply Orange Pulp Free Orange Juice, 46 FL OZ (1.4 QT) 1.36 L, packaged in a plastic bottle, UPC: 025000136788 2) Simply Orange Pulp Free Orange Juice, 11.5 FL OZ (340 mL), packaged in a plastic bottle, UPC: 025000000249
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0402-2025·2025-08-13

    Clover Valley lactose free milk recalled after a temperature excursion

    Clover Valley Lactose Free 2% Reduced Fat Milk, 64 fl oz, is being recalled because of temperature abuse following a temperature excursion in one shipping trailer. 1 unit is affected.

    Product
    Clover Valley Lactose Free 2% Reduced Fat Milk, 64 FL OZ (2 QTS) 1.89 L, packaged in a paper carton, UPC: 070744010085
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0571-2025·2025-08-13

    Xolair auto-injectors exposed to temperatures outside labeled storage requirements

    Xolair (omalizumab injection) 150 mg/mL auto-injectors are being recalled because of CGMP deviations: the product was exposed to temperatures outside its labeled storage requirements. 6 units affected.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide