The Recall Desk

Hazard

Microbial Contamination recalls

1,320 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,320
Critical
313
Severe
670
Most recent
2026-09-09

Of the 1,320 microbial contamination recalls we have scored against our rubric, 313 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 670 (51%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all microbial contamination recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

926–950 of 1320

  • ModerateFDA (Food)·F-0350-2018·2017-11-15

    Harmless Harvest Recalls Probiotic Drinks Due to Premature Spoilage

    Harmless Harvest is recalling four varieties of probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.

    Product
    Harmless Coconut Probiotics Strawberries; Coconut Cultured Beverage; UPC 859078-002566; Keep refrigerated 11 lf. oz. HDPE Bottle Ingredients: Organic Coconut Water, Water, Organic Coconut Meat, Organic Cane Sugar, Organic Strawberries, live and active cultures. Harmle
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0351-2018·2017-11-15

    Harmless Harvest Recalls Probiotic Drinks Due to Premature Spoilage

    Harmless Harvest is recalling four varieties of Probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.

    Product
    Harmless Coconut Probiotics Blueberries & A¿a¿; Coconut Cultured Beverage; UPC 859078-002702; 11 lf. oz. HDPE Bottle; Keep refrigerated Ingredients: Organic Coconut Water, Water, Organic Coconut Meat, Organic Cane Sugar, Organic Blueberries, Organic Acai, live and active
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-3545-2017·2017-09-20

    Monster Energy Recalls Java Monster Loco Moca Coffee Due to Processing Error

    Monster Energy Company is recalling Java Monster Loco Moca Coffee & Energy because the product was distributed without undergoing the required retort step.

    Product
    Java Monster Loco Moca Coffee & Energy, Net Wt. 15 fl. oz. (443 mL); UPC 0 70847 81271 5; INGREDIENTS: BREWED COFFEE (FILTERED WATER., COFFEE, CONDENSED SKIM MILK. SUGAR, HEAVY CREAM. GLUCOSE. NATURAL FLAVORS. TAURlNE,. SODIUM CITRATE, MICiOCRYSTALLINE CELLULOSE. PANAX GI
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1141-2017·2017-09-20

    Centurion Labs Recalls Ninjacof-A Oral Solution Due to Microbial Contamination

    Centurion Labs is recalling Ninjacof-A oral solution due to potential B. cepacia contamination. Consumers should stop using the product and return it to the pharmacy.

    Product
    Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-033-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1122-2017·2017-08-30

    Rugby Aller-chlor Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1123-2017·2017-08-30

    Rugby Senexon Liquid Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1120-2017·2017-08-30

    Rugby Diocto Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1121-2017·2017-08-30

    Major Senna Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1119-2017·2017-08-30

    Rugby Diocto Liquid Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1052-2017·2017-08-09

    VistaPharm Recalls Lactulose Solution Due to Microbial Contamination

    VistaPharm is recalling Lactulose Solution, USP, because the product failed microbial testing for yeast and mold counts.

    Product
    Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by VistaPharm, Inc., Largo, FL 33771, NDC 66689-038-50
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-1054-2017·2017-08-09

    Vi-Jon Recalls Magnesium Citrate Oral Solution Due to Mold Contamination

    Vi-Jon, Inc. is recalling 101,244 bottles of Magnesium Citrate Oral Solution because the product was found to contain mold identified as Rhinocladiella similis.

    Product
    Magnesium Citrate Oral Solution, packaged in a 10 fl. oz. (296 mL) glass bottle, OTC, labeled as: a) GoodSense Magnesium Citrate Oral Solution Saline Laxative Very Low Sodium, UPC# 846036007381, NDC 50804-686-38, Distributed by: Geiss, Desitin &Dunn, Inc., Peachtree City, GA 3026
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1053-2017·2017-08-09

    VistaPharm Recalls Lactulose Solution Due to Microbial Contamination

    VistaPharm is recalling Lactulose Solution, USP, because the product failed microbial testing for yeast and mold counts.

    Product
    Lactulose Solution, USP, 20 g/30 mL, dose cups delivers 30 mL packaged 50-unit dose cups per case, Manufactured by VistaPharm, Inc., Largo, FL 33771, NDC 66689-038-01
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0975-2017·2017-07-19

    CVS Health Baby Eczema Moisturizing Cream Recalled for Microbial Contamination

    Sigan Industries is recalling CVS Health Baby Eczema Moisturizing Cream due to microbial contamination. The product failed to meet total plate count specifications.

    Product
    CVS Health Baby Eczema Moisturizing Cream(colloidal oatmeal 1.0%), Net Wt. 7.3 oz (207g) tubes, OTC, Distributed by CVS Pharmacy Inc., Woonsocket, RI --- UPC 050428568033
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0899-2017·2017-06-21

    Bausch & Lomb Recalls NasalCrom Nasal Spray Due to Potential Microbial Contamination

    Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.

    Product
    NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered sprays, 0.88 FL OZ (26 mL) metered spray pump bottle, Distributed by: Medtech Products, Inc., Tarrytown, NY 10591, UPC 8 148332 01101 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2180-2017·2017-06-07

    Vascular Solutions Recalls Dolphin Inflation Devices Due to Sterile Barrier Defect

    Vascular Solutions, Inc. is recalling 4,110 Dolphin Inflation Devices due to a potential sterile barrier defect that could lead to microbial contamination and infection.

    Product
    Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile inflation device used in cardiovascular procedures to pressurize (inflate) and depressurize (deflate) balloon catheters. The device itself consists of two compo
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Drugs)·D-0856-2017·2017-05-31

    Sato Pharmaceutical Recalls DORAMA-NEO Eye Wash Due to Sterility Concerns

    Sato Pharmaceutical Inc. is recalling 14,325 bottles of DORAMA-NEO eye wash because the manufacturer failed to establish an adequate system for monitoring environmental conditions in aseptic processing areas.

    Product
    DORAMA-NEO (naphazoline hydrochloride) Eye wash, packaged in 0.5 FL OZ (15mL) bottles, Manufactured by SATO Pharmaceuticals CO., LTD. 1-5-27 Motoakasaka Minato-Ku Tokyo, Japan, NDC 49873-020-01
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0705-2017·2017-05-17

    Teva Recalls Clozapine Tablets Due to Microbial Contamination

    Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.

    Product
    Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem, 977
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2149-2017·2017-05-03

    USN B4 Bomb Extreme Pre-Workout Recalled for Staphylococcus Aureus Concern

    Armada Nutrition is recalling USN B4 Bomb Extreme Pre-Workout due to a raw material testing failure for Staphylococcus aureus that was not fully investigated.

    Product
    USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300g, USN North America, 1560 Sawgrass Corporation Pkwy, 4th Floor, Sunrise, FL, 33323
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0662-2017·2017-04-19

    Signature Club A Recalls Double Hyaluronic 1000 Day Cream for Microbial Contamination

    Signature Club A Ltd is recalling 1,237 jars of Double Hyaluronic 1000 Volumizing Day Cream due to microbial contamination.

    Product
    Double Hyaluronic 1000, 'AN OUNCE OF GOLD' Volumizing Day Cream, Broad Spectrum SPF 30+, (Octinoxate 7.725%, Oxybenzone 6.18%, Octisalate 5.15%, Avobenzone 3.09%), Net Wt. 1.8 oz. (51 g) jar, Distributed by Signature Club A, Ltd, Tampa, FL 33609.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0622-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Institutional, Inc. is recalling 1,527 cartons of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0621-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets, 80 mg, due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 80 mg*, packaged in a) 90-count bottles (NDC 0378-3953-09) and b) 500-count bottles (NDC 0378-3953-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0618-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 10 mg*, packaged in a) 90-count bottles (NDC 0378-3950-77); b) 90-count bottles (NDC 0378-3950-09); c) 500-count bottles (NDC 0378-3950-05); d) 500-count bottles (NDC 0378-3950-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0619-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets 20 mg due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 20 mg*, packaged in a) 90-count bottles (NDC 0378-3951-09) and b) 500-count bottles (NDC 0378-3951-07); Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide