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.

276–300 of 1320

  • CriticalFDA (Drugs)·D-0218-2021·2021-01-06

    Wishgarden Herbs Recalls Happy Ducts Compress Due to Microbial Contamination

    Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.

    Product
    Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0220-2021·2021-01-06

    WishGarden Herbs Recalls Goldenseal Powder Jars Due to Microbial Contamination

    WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.

    Product
    Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0219-2021·2021-01-06

    Recall of Cord Care Powder Due to Cronobacter Sakazakii Contamination

    A non-sterile Cord Care Powder product was recalled because testing found Cronobacter Sakazakii contamination, posing a potential health risk without confirmed illness reports.

    Product
    Cord Care POWDER, 0.25 oz. (7 g) plastic jars, Wishgarden Herbs, Inc., Boulder, CO 80301. UPC 6-56490 24730 4
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0653-2021·2020-12-30

    CryoLife Recalls CryoPatch SG Pulmonary Human Cardiac Patch Units

    CryoLife, Inc. is recalling two units of CryoPatch SG Pulmonary Human Cardiac Patch due to post-processing microbial culture test failures.

    Product
    CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch of a three-pouch packaging system. The packaging system not only withstands ultracold temperatures, but also allows for aseptic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0652-2021·2020-12-30

    CryoLife Recalls CryoValve SG Pulmonary Heart Valves Due to Microbial Test Failures

    CryoLife, Inc. is recalling three CryoValve SG Pulmonary Human Heart Valves because post-processing microbial culture tests failed for allografts processed with the same TRIS saline solution lot.

    Product
    CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing cryoprotectants within the innermost pouch of a three-pouch packaging system. The packaging system not only withstands ultracold temperatures, but also allows for aseptic i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2021·2020-12-16

    TissueTech Recalls PROKERA Slim Corneal Bandages Due to Microbial Contamination

    TissueTech, Inc. is recalling 75 units of PROKERA Slim non-sterile biologic corneal bandages due to potential exposure to microbial contamination.

    Product
    PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0111-2021·2020-12-09

    Lohxa Recalls Chlorhexidine Gluconate Oral Rinse Due to Bacterial Contamination

    Lohxa LLC is recalling Chlorhexidine Gluconate Oral Rinse USP, 0.12%, due to contamination with Burkholderia lata bacteria.

    Product
    Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715), packaged in 50-count unit dose cups per carton, Rx only, Distributed by: Lohxa, Worcester, MA 01608, NDC 70166-027-15
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0103-2021·2020-12-02

    Paroex Oral Rinse Recalled for Burkholderia lata Contamination

    Sunstar Americas is recalling Paroex Oral Rinse due to microbial contamination with Burkholderia lata. The recall covers specific lots distributed nationwide.

    Product
    Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1584-2020·2020-09-23

    Maison Terre Goldenseal Root Powder Recalled for Microbial Contamination

    Maison Terre, LLC is recalling Goldenseal Root Powder Organic due to FDA findings of contamination with various microorganisms, including Cronobacter sakazakii.

    Product
    Goldenseal Root Powder Organic, 1 oz. clear plastic bag, Maison Terre Natural Products, www.maisonterre.net
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1534-2020·2020-09-02

    Medichem Recalls Chlorhexidine Gluconate Due to Serratia marcescens Contamination

    Medichem S.A. is recalling Chlorhexidine Gluconate 0012 for manufacturing due to microbial contamination with Serratia marcescens.

    Product
    Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking, RX Only, Medichem, S.A. Poligono Industrial Celra, 17460, Celra, Girona (Spain/Espana); Fructuos Gelabert, 6-8, 08970, Sant Joan Despi, Barcelona (Spain/Espana) NDC 53296-0012-0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1503-2020·2020-08-12

    Spartan Chemical Recalls Lemon Blossom Hand Sanitizer Due to Microbial Contamination

    Spartan Chemical Co Inc is recalling Lemon Blossom Hand Sanitizer because testing found positive microbial contamination in the product.

    Product
    Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For Institutional and Industrial Use Only, a) foamyiQ 42.27 oz/1250 mL cartridge, UPC code: 7 53727 26454 4; b) Lite 'n Foamy 1 gallon/3.79 L container UPC code: 7 53727 26113 0, Spartan Chemical Company,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1241-2020·2020-04-22

    Dermatone Sunscreen Recalled for Microbial Contamination

    Filltech USA is recalling Dermatone Sunscreen Lotion due to positive tests for yeast and bacteria.

    Product
    Dermatone (avobenzone, homosalate, octisalate, and octocrylene) Sunscreen Lotion Fragrance Free, SPF 30, package in 1.5 fl. oz. (44 mL) tottles, Distributed By: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 020908422698
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1242-2020·2020-04-22

    Dermatone Sunscreen Recalled for Microbial Contamination

    Filltech USA is recalling Dermatone Sunscreen Lotion SPF 50 due to positive tests for yeast and bacteria.

    Product
    Dermatone (avobenzone, homosalate, octisalate, and octocrylene) Sunscreen Lotion Fragrance Free, SPF 50, packaged in a) 1.5 fl. oz. (44 mL) tottles, UPC: 087052727338; b) 2 Fl. OZ. (59 mL) tubes, UPC: 08705272732; c) 4 FL. OZ. (118 mL) tubes, UPC: 087052727345, Distributed By: Be
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0847-2020·2020-02-19

    Efficient Laboratories Recalls Rompe Pecho MAX Due to Microbial Contamination

    Efficient Laboratories, Inc. is recalling 4,080 bottles of Rompe Pecho MAX Multi Symptoms due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.

    Product
    New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 00309 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0846-2020·2020-02-19

    Rompe Pecho EX Expectorant Recalled for Microbial Contamination

    Efficient Laboratories, Inc. is recalling 5,387 bottles of Rompe Pecho EX Expectorant due to microbial contamination. Consumers should stop using the product and return it to the place of purchase.

    Product
    Rompe Pecho EX Expectorant, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 30106 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0845-2020·2020-02-19

    Efficient Laboratories Recalls Rompe Pecho CF Cold & Flu Due to Microbial Contamination

    Efficient Laboratories is recalling 5,249 bottles of Rompe Pecho CF Cold & Flu with Honey due to microbial contamination. The product was distributed nationwide in the USA.

    Product
    Rompe Pecho CF Cold & Flu with Honey, 6 FL. Oz (178 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166.UPC 0 00856 33106 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0838-2020·2020-01-29

    Imactis Navigation Kit Recalled for Potential Microbial Contamination

    Imactis is recalling 122 Navigation Kits because the sensor cover may contain microbial contamination, posing a risk of pyrogenic response.

    Product
    Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref. A10010 CE 0459, Sensor Cover Ref. PC3688 CE 0482, Adhesif Film Ref. 38.20.15 CE 0459, EN Navigation Kit. Compatible with linear instruments of diameter ranging from 0.5 mm to 3.0 mm (25G to 11G), Sterile, Rx On
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0782-2020·2020-01-22

    Sigan Eczema Skin Relief Lotion Recalled for Microbial Contamination

    Sigan Industries is recalling Eczema Skin Relief Lotion due to microbial contamination. The product was distributed in Illinois.

    Product
    Eczema Skin Relief Lotion, 2% Colloidal Oatmeal Skin Protectant Lotion, NET WT 14 OZ (396 g), NDC 65365-266-01, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0630-2020·2019-12-25

    Lannett Recalls Levetiracetam Oral Solution Due to Microbial Contamination

    Lannett Company is recalling specific lots of Levetiracetam Oral Solution because testing found out-of-specification microbial counts.

    Product
    Levetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed by: Lannett Company, Inc. Philadelphia, PA 19136, NDC 54838-0548-80
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0609-2020·2019-12-11

    Lens.com Recalls Alcon Air Optix Night & Day Aqua Contact Lenses

    Lens.com is recalling specific lots of Alcon Air Optix Night & Day Aqua contact lenses because they may be counterfeit and have microbial issues.

    Product
    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0533-2020·2019-12-11

    Fagron Recalls LETS GEL Kits Due to Microbial Contamination

    Fagron, Inc. is recalling 11,912 kits of LETS GEL Convenience Packs due to microbial contamination of the non-sterile product.

    Product
    LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL), Contains: LETS Powders for Gel: Lidocaine Hydrochloride - 4 g, Ephinephrine Bitartrate - 180 mg, Tetracaine Hydrochloride - 500 mg, Sodium Metabisulfite - 75 mg, SuturaGel Methlcellulose Base; RX Only, For Prescription
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0126-2020·2019-10-16

    Major Infants' Gas Relief Drops Recalled for Microbial Contamination

    GCP Laboratories is recalling Major Infants' Gas Relief Drops due to microbial contamination of the non-sterile product.

    Product
    Major Infants' Gas Relief Drops, Simethicone Oral Suspension USP, 1 FL OZ (30 mL) bottle, Distributed by: Major Pharmaceuticals 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152 USA. NDC 0904-5894-30
    Category
    Drug
    Distribution
    Distributed nationwide