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Recalls affecting Louisiana

Data last updated: September 8, 2026 at 1:13 PM UTC

16,895 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

▸Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

▸Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

▸Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

▸Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

▸Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
NewestOldest
High riskLow riskAll
Wording
Class IIModerate risk
DrugRecalled September 30, 2022

Flunisolide Nasal Solution, USP 0.025%, 25 mL bottles, Rx only, Manufactured for: Ingenus Pharmaceuticals, LLC Orlando, FL 32839-6408; NDC 50742-317-25 UPC 3 50742 31725 7

Not meeting quality requirements for related substances (impurities).

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0010-2023
Lot/product code:
Lot #: 22E040 Exp. 07/2023; 22F038 Exp. 08/2023
Recalling firm:
Ingenus Pharmaceuticals Llc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 5, 2022

Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, Made in India, NDC 65862-162-90

CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0021-2023
Lot/product code:
Lots QE2021005-A and QE2021010-A, exp 01/2023
Recalling firm:
Aurobindo Pharma USA Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PAPAVERINE / PHENTOLAMINE INJECTION 150MG / 5MG / VIAL SOLUTION, 10 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0046-2023
Lot/product code:
Lots: 55092, BUD: 10/22/2022; 59100, BUD: 10/30/2022; 62038, BUD: 04/08/2023; 66533, BUD: 04/08/2023
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

TALC, STERILE POWDER, 5 GM vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0055-2023
Lot/product code:
Lot: 65995, BUD: 10/28/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

AUTOLOGUS TEARS SERUM SOLN FULL STRENGTH, 3 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0028-2023
Lot/product code:
Lots: 65521, BUD: 10/15/2022; 65545, BUD: 10/15/2022; 65605, BUD: 10/16/2022; 65658, BUD: 10/17/2022; 65733, BUD: 10/21/2022; 65894, BUD: 10/24/2022; 66019, BUD: 10/28/2022; 66120, BUD: 10/30/2022; 66388, BUD: 11/6/2022; 66755, BUD: 11/14/2022; 66870, UD: 11/18/2022; 66928, BUD: 11/19/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PAP/PHEN/PROSTAG/ATROPINE INJ 150MG/7.5MG/75MCG/1MG bottle solution, 5 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0041-2023
Lot/product code:
Lots: 66369, BUD: 11/06/2022; 66540, BUD: 11/09/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

LIDOCAINE/PHENYLEPHRINE PF SYR 1%/1.5% Solution, 3 mL syringes, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0035-2023
Lot/product code:
Lot: 65972, BUD: 10/27/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

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

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0040-2023
Lot/product code:
Lot: 66470, BUD: 11/10/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN INJ 90MG/3MG/29.4MCG/ BOTTLE SOLUTION, 5 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0045-2023
Lot/product code:
Lots: 66450, BUD: 11/07/2022; 66527, BUD: 11/09/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PAPAVERINE HCL STOCK SOLUTION 30MG/ML SOLUTION, 10 mL vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0047-2023
Lot/product code:
Lot: 60552, BUD: 03/12/2023
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled October 7, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084

During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.

ALARAZCACOCTDCDEFLGAIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVTWAWIWVWY
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0065-2023
Lot/product code:
Enjoy By Dates of Oct. 28, Oct. 31, Nov. 4, and Nov. 7; Product Codes 307 2263 through 307 2274
Recalling firm:
Flowers Foods (Corporate Offices)
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

SERUM TEARS IN NSAL 20% OPTH SOLUTION, 3 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0054-2023
Lot/product code:
Lots: 65490, BUD: 10/14/2022; 65584, BUD: 10/16/2022; 66013, BUD: 10/28/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PAPAVERINE/PHENTOLAMINE/PROSTAGLANDIN INJ 150MG/5MG/10MCG/VIAL SOLUTION, 5 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0049-2023
Lot/product code:
Lot: 65976, BUD: 10/27/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled October 7, 2022

TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 00972 7 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112

During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.

ALARAZCACOCTDCDEFLGAIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVTWAWIWVWY
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0067-2023
Lot/product code:
Enjoy By Dates of Oct. 28, Oct. 31, Nov. 4, and Nov. 7; Product Codes 307 2263 through 307 2274
Recalling firm:
Flowers Foods (Corporate Offices)
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled October 7, 2022

TASTYKAKE GLAZED LEMON FLAVORED PIE NET WT 4.5 OZ (128g) UPC 0 25600 00967 3 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112

During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.

ALARAZCACOCTDCDEFLGAIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVTWAWIWVWY
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0070-2023
Lot/product code:
Enjoy By Dates of Oct. 28, Oct. 31, Nov. 4, and Nov. 7; Product Codes 307 2263 through 307 2274
Recalling firm:
Flowers Foods (Corporate Offices)
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled October 7, 2022

TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 08618 6 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112

During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.

ALARAZCACOCTDCDEFLGAIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVTWAWIWVWY
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0068-2023
Lot/product code:
Enjoy By Dates of Oct. 28, Oct. 31, Nov. 4, and Nov. 7; Product Codes 307 2263 through 307 2274
Recalling firm:
Flowers Foods (Corporate Offices)
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

LIDOCAINE EPINEPHRINE BUFFERED 2%/1:1000 Solution, 10 mL syringe, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0036-2023
Lot/product code:
Lot: 66591, BUD: 11/12/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

CYCLOSPORIN 0.07% OPTH 0.07% Solution in 10 mL bottles, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0032-2023
Lot/product code:
Lots: 59638, BUD: 11/25/2022; 64261, BUD: 04/30/2023
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

CEFUROXIME INTRAVITREAL SYR 1MG/0.1ML Solution in 1 mL syringe, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0031-2023
Lot/product code:
Lots: 63265, BUD: 01/24/2023; 66085, BUD: 04/03/2023
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

ACETYLCYSTEINE OPTH 10% Solution, 15 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0026-2023
Lot/product code:
Lot: 66895, BUD: 11/19/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

ACETYLCYSTEINE OPTH 5% Solution, 15 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0027-2023
Lot/product code:
Lots: 66017, BUD: 10/13/2022; 66177, BUD: 10/19/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

METHYLCOBALAMIN PF 1 ML Injection Solution 5,000 MCG/ML Solution, 1 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0038-2023
Lot/product code:
Lot: 57997, BUD: 02/25/2023; 64941, BUD: 03/08/2023
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0051-2023
Lot/product code:
Lots: 65056, BUD: 11/18/2022; 66246, BUD: 11/19/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

PROSTAGLANDIN E1 INJECTION SOLUTION 500MCG/ML SOLUTION, 1 ML vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0052-2023
Lot/product code:
Lots: 59993 BUD: 10/18/2022; 60932 BUD: 11/09/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 7, 2022

BRILLIANT BLUE G, 0.04% Solution, 2 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402

Not guaranteed to be germ-free: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

ALLAMSTN
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0029-2023
Lot/product code:
Lot: 60448 BUD: 10/31/2022
Recalling firm:
Pharmacy Plus, Inc. dba Vital Care Compounder
View official FDA record (opens in a new tab)