State

Louisiana product recalls

73,381 recalls have nationwide distribution and so reach Louisiana. 6,958 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,958
Critical: 1,109
Severe: 1,737
Most recent: 2026-09-23

Of the 6,958 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,737 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,958 recalls whose distribution notice names Louisiana specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19851–19875 of 80339

SevereFDA (Food)·F-0111-2023·2022-11-09
Multiple Brands of Baked Brie Cheese Recalled for Listeria Contamination Risk
Multiple brands of baked brie cheese are being recalled due to potential Listeria monocytogenes contamination. Products were distributed across multiple U.S. states and Mexico.
Product
Reny Picot 8 oz Baked Brie, Plain UPC 033421050088 Mexideli 12 oz Baked Brie, Plain no UPC N/A LA BONNE VIE 8 oz Baked Brie, Plain UPC 820581678814 PRIMO TAGLIO 8 oz Baked Brie, Plain UPC 021130098460
Category
Food
Distribution
25 states
SevereFDA (Food)·F-0113-2023·2022-11-09
Reny Picot Apple Baked Brie recalled for potential Listeria contamination
Old Europe Cheese, Inc. is recalling Reny Picot Apple Baked Brie due to potential Listeria monocytogenes contamination. The recall affects 1,309 pieces with best-by dates from September 28, 2022 to December 14, 2022.
Product
Reny Picot 11 oz Apple Baked Brie UPC 033421500811
Category
Food
Distribution
25 states
SevereFDA (Food)·F-0118-2023·2022-11-09
Saint Louis Brie Products Recalled Due to Potential Listeria Contamination
Saint Louis Brie and related brie products have been recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,701 cases distributed to retailers in Louisiana, Maine, Missouri, North Carolina, and New York.
Product
Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint Louis Domestic Cut Brie Wedge, variable weight-6lb RD WT, saran wrapped, UPC: 041563 370018; Saint Louis Brie, variable weight, saran wrapped, UPC: 21107100000; Saint Louis CW Brie Wheel, 1/3 KG RD…
Category
Food
Distribution
5 states
HighNHTSA·22V832000·2022-11-09
Motorhome interior step tread may detach, increasing fall injury risk
Holiday Rambler and Fleetwood motorhomes (2022–2023) have interior step treads that may be improperly secured and can detach when stepped on, creating a fall hazard.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD INVICTA, VACATIONER, BOUNDER, FORTIS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0158-2023·2022-11-09
Surgical Cataract Pack Recalled Due to Compromised Sterile Packaging
Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.
Product
BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0082-2023·2022-11-09
Domino and C&H Sugar recalled for potential metal wire contamination
Domino Foods Inc is recalling Domino and C&H Granulated Pure Cane Sugar (Easy Baking Tub) due to potential contamination with metal wire from a broken screen. The recalled product was distributed to distribution centers in 22 states.
Product
Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case
Category
Food
Distribution
22 states
HighFDA (Food)·F-0120-2023·2022-11-09
Cottage Cheese Products Recalled for Possible Plastic Foreign Objects
Multiple cottage cheese brands are recalled due to possible plastic foreign objects. The recall affects 391,824 cases distributed to 38 states.
Product
Hannaford Cottage Cheese, 16oz and 24 oz; Hood Country Style Cottage Cheese, 16 oz, 24 oz., 32 oz.; Hood Large Curd Cottage Cheese, 16 oz; IGA Cottage Cheese, 16 oz; IGA Large Curd Cottage Cheese, 16 oz; Market Basket Cottage Cheese, 16 oz, 24 oz; Weis Cottage Cheese, 16 oz and…
Category
Food
Distribution
39 states
HighFDA (Food)·F-0123-2023·2022-11-09
Hood Cottage Cheese with Blueberries Recalled for Plastic Contamination
HP Hood LLC is recalling Hood Cottage Cheese with Blueberries (16 oz) because the product may contain plastic pieces. Affected products have best-by dates between October 24, 2022 and December 12, 2022.
Product
Hood Cottage Cheese with Blueberries, 16 oz
Category
Food
Distribution
39 states
HighFDA (Devices)·Z-0172-2023·2022-11-09
BD Trucount Tubes Recalled Due to Partial Label Detachment Causing Operational Failures
Becton Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together in pouches or fail when used with automated loaders. No illnesses have been reported.
Product
BD Trucount Tubes (Cat. No. 663028), used for determining absolute counts of leukocytes in blood. BD Trucount Tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount Tubes can be used with the…
Category
Medical Device
Distribution
43 states
HighFDA (Food)·F-0125-2023·2022-11-09
Hood and Penn Maid Cottage Cheese Recalled for Possible Plastic Contamination
HP Hood LLC is recalling Hood and Penn Maid cottage cheese with pineapple and cherry due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.
Product
Hood Cottage Cheese with Pineapple & Cherry, 16 oz; Penn Maid Cottage Cheese with Pineapple & Cherry, 16 oz
Category
Food
Distribution
39 states
HighFDA (Drugs)·D-0030-2023·2022-11-09
Ceftazidime Intravitreal Solution Recalled for Sterility Assurance Failure
Vital Care Compounder is recalling Ceftazidime intravitreal injection solutions due to manufacturing conditions that cannot guarantee product sterility. Affected lots were distributed to patients in Alabama, Louisiana, Mississippi, and Tennessee.
Product
CEFTAZIDIME INTRAVITREAL 2.25MG/0.1ML Solution, 0.5 mL syringe, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0044-2023·2022-11-09
Compounded Injectable Drug Recalled Due to Sterility Assurance Defect
A compounded injectable medication containing papaverine, phentolamine, and prostaglandin was recalled after FDA inspection found it was not produced under conditions that guarantee sterility. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN INJ 75MG/2.5MG/50MCG/ BOTTLE SOLUTION, 5 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Devices)·Z-0170-2023·2022-11-09
Aneurysm Embolization System Detachment Controller Recalled for Manufacturing Defect
MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.
Product
WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm Embolization System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0042-2023·2022-11-09
Pharmacy Plus Injectable Drug Recall Due to Sterility Assurance Failure
Pharmacy Plus, Inc. recalled a compounded injectable medication (56 vials) due to manufacturing processes that cannot guarantee product sterility. Distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN 150MG / 2.5MG / 50MCG SOLUTION, 5 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0051-2023·2022-11-09
Prescription eye drops recalled due to sterility assurance defect
Vital Care Compounder is recalling 378 droptainers of PRED ACETATE/GATIFLOXACIN eye drops distributed in AL, LA, MS, and TN due to inability to guarantee manufacturing sterility. No illnesses have been reported.
Product
PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Devices)·Z-0157-2023·2022-11-09
Bausch + Lomb Ophthalmic Surgical Kits Recalled for Sterile Packaging Defect
Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.
Product
BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0106-2023·2022-11-09
Bella Cucina Walnut Sage Pesto recalled for undeclared milk allergen
Bella Cucina Artful Food is recalling Walnut Sage Pesto because milk is present in the product but not declared on the label. Consumers allergic to milk should not consume this product.
Product
Bella Cucina Artful Food Walnut Sage Pesto Net Wt. 6 oz (169g) glass jar, UPC 6 19193 00041 6 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0124-2023·2022-11-09
Hood Cottage Cheese Recalled for Possible Plastic Contamination
HP Hood is recalling Hood Cottage Cheese with Cucumber & Dill (16 oz) because the product may contain plastic foreign objects. Consumers should not eat the recalled product.
Product
Hood Cottage Cheese with Cucumber & Dill, 16 oz
Category
Food
Distribution
39 states
HighFDA (Drugs)·D-0035-2023·2022-11-09
Lidocaine/Phenylephrine Injectable Solution Recalled for Sterility Defect
Pharmacy Plus Inc.'s Lidocaine/Phenylephrine injectable solution is recalled due to manufacturing process deficiencies that cannot guarantee product sterility. The recall affects 389 syringes distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
LIDOCAINE/PHENYLEPHRINE PF SYR 1%/1.5% Solution, 3 mL syringes, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0034-2023·2022-11-09
Laureth-9 Injectable Solution Recalled for Lack of Sterility Assurance
A compounded Laureth-9 injectable solution has been recalled after the FDA found the manufacturing process could not guarantee sterility. The recalled product (lot 66513) was distributed in AL, LA, MS, and TN.
Product
LAURETH-9 INJ 2% Solution, 30 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Drugs)·D-0057-2023·2022-11-09
Voriconazole ophthalmic solution recalled for sterility concerns
Pharmacy Plus, Inc. (Vital Care Compounder) is recalling Voriconazole Ophthalmic Solution 2% because FDA inspection found manufacturing processes cannot guarantee the product's sterility.
Product
VORICONAZOLE OPTH SOLUTION 2% STERILE SOLN, 10 ML droptainer, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Devices)·Z-0171-2023·2022-11-09
BD Trucount Tubes for Blood Testing Recall Due to Label Detachment
Becton, Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together or create automation errors. The defect stems from an adhesive supplier change and affects 52,570 units.
Product
BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped flow cytometer. BD Trucount tubes can be used with the…
Category
Medical Device
Distribution
43 states
HighFDA (Drugs)·D-0040-2023·2022-11-09
Moxifloxacin Preservative-Free Eye Drops Recalled for Sterility Assurance Failure
Pharmacy Plus, Inc. is recalling Moxifloxacin 0.15 mg/0.1 mL preservative-free eye drops in 1 mL syringes due to lack of assured sterility. FDA inspection found the manufacturing process could not guarantee the product's sterility.
Product
MOXIFLOXACIN PRESERVATIVE FREE SYR, 0.15 mg/0.1 mL, Sterile Solution, 1 mL syringes, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Category
Drug
Distribution
4 states
HighFDA (Food)·F-0126-2023·2022-11-09
Hood Cottage Cheese with Strawberries Recalled for Plastic Foreign Objects
HP Hood LLC is recalling 391,824 cases of Hood Cottage Cheese with Strawberries (16 oz) due to possible plastic foreign object contamination.
Product
Hood Cottage Cheese with Strawberries; 16 oz
Category
Food
Distribution
39 states
HighNHTSA·22V830000·2022-11-09
2023 Volkswagen ID.4 electric motor coolant leak risk
Volkswagen is recalling 2023 ID.4 vehicles due to improper electric motor sealing assembly that may allow coolant to leak into the high-voltage system, risking loss of vehicle control and unintended airbag deployment.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide