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.

1026–1050 of 1320

  • CriticalFDA (Drugs)·D-450-2015·2015-04-15

    Central Admixture Pharmacy Services Recalls Non-Sterile Neonatal TPN Bags

    Central Admixture Pharmacy Services is recalling four bags of neonatal TPN due to non-sterility test failures. The product was distributed nationwide.

    Product
    Sinai Hospital (MD) TPN Neonatal Day 1 Bag, Trophamine 10 g, Dextrose 25 g, Additives: Calcium Gluconate 1500 mg, compound vol: 250 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is lined with a polystyrene insert; C
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-468-2015·2015-04-15

    FDA Recalls Two Bags of Neonatal TPN Due to Sterility Failure

    Central Admixture Pharmacy Services is recalling two bags of a compounded neonatal TPN product because sterility testing failed. The product was distributed nationwide.

    Product
    Spotsylvania Regional Med Ctr (VA) TPN Neonatal Starter Bag with Calcium, Trophamine 5 gm, Dextrose 10%, Additives: Calcium Gluconate 0.46 mEq/mL, 750mg, compound vol: 250 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each contai
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-464-2015·2015-04-15

    CAPS Recalls Lankenau Hospital TPN Neonatal Starter Bags for Sterility Failure

    Central Admixture Pharmacy Services is recalling six Lankenau Hospital TPN Neonatal Starter Bags due to out-of-specification sterility test results.

    Product
    Lankenau Hospital (PA) TPN Neonatal Starter Bag, Trophamine 2.5%, Dextrose 10%, Additives: heparin PF 62.5 units, Calcium Gluconate 500mg, compound vol: 250 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is lined wit
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0419-2015·2015-03-25

    Tarmac Recalls Antacid Liquid Due to Microbial Contamination

    Tarmac Products is recalling specific lots of Antacid Liquid Regular Strength because they failed microbiological testing at the 12-month time point.

    Product
    Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200 mg, Magnesium hydroxide 200 mg, Simethicone 20 mg (in each 5 mL, 1 teaspoon), Mint flavor, 12 fl oz (355 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0073-02, UP
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0410-2015·2015-03-18

    Fusion Pharmaceuticals Recalls Contaminated Diphenhydramine Oral Suspension Kits

    Fusion Pharmaceuticals is recalling 9,439 kits of Dicopanil oral suspension due to microbial contamination with Burkholderia multivorans. The affected kits were distributed in California.

    Product
    DICOPANOL (diphenhydramine hydrochloride in 5 mg/mL oral suspension kit) FusePaq, 150 mL Kits, Rx Only. Fusion Pharmaceuticals LLC., 768 Calle Plano, Camarillo, CA 93012. NDC: 43093-104-01.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0385-2015·2015-02-18

    Akorn Recalls Erythromycin Pledgets Due to Microbial Contamination

    Akorn, Inc. is recalling Erythromycin Pledgets USP, 2%, 60-count jars because the active pharmaceutical ingredient failed USP microbial tests.

    Product
    Erythromycin Pledgets USP, 2%, 60-count jar,Rx only, Manufactured by Ei LLC, Kannapolis, NC 28083, Marketed by VersaPharm Incorporated, Marietta, GA 30062, NDC 61748-202-60 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0379-2015·2015-01-28

    Valeant Recalls Virazole Due to Microbial Contamination

    Valeant Pharmaceuticals is recalling Virazole (ribavirin) inhalation solution due to positive microbial contamination found during stability testing.

    Product
    Virazole (Ribavirin for Inhalation Solution, USP), Sterile Lyophilized For Administration by Aerosol Inhalation Only, Rx only, Contents: Four 6 g vials, 100 mL, Distributed by: Valeant Pharmaceuticals North America, Bridgewater, NJ 08807 USA, NDC 0187-0007-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0328-2015·2015-01-07

    Tropichem Recalls Entertainer's Secret Throat Relief Due to E. Coli Contamination

    Tropichem Research Labs is recalling Entertainer's Secret Throat Relief due to microbial contamination, including E. Coli. The product was distributed in New York and Indiana.

    Product
    Entertainer's Secret Throat Relief, 2.0 FL oz (59.2 mL), Honey Apple Flavor, KLI Corp, Carmel, IN
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0495-2015·2014-11-19

    Exotic Superfoods Recalls Raw Thai Coconut Water Due to Processing Failure

    Exotic Superfoods New York, Inc. is recalling specific lots of 100% Raw Young Thai Coconut Water because the batches were not subjected to the required 5-log reduction processing.

    Product
    Exotic Superfoods 100% Raw Young Thai Coconut Water, 32 oz. SKU: 7 05105 50171 0 Exotic Superfoods 100% Raw Young Thai Coconut Water, 11.7 oz. SKU: 7 05105 50161 1 Description of the Product: - 32 oz (1 quart): - The product is consumed in individual clear plastic bot
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0230-2015·2014-11-05

    FDA Recalls Calcium Glucosate Injection Due to Microbial Contamination

    Specialty Compounding, LLC is recalling Calcium Gluconate 2 gm in 100 mL Sodium Chloride 0.9% for Injection due to non-sterility and microbial contamination.

    Product
    CALCIUM GLUCONATE 2 gm (PF) PRESERVATIVE FREE in 100 mL Sodium Chloride 0.9% for Injection, Rx Only Manufactured by Specialty Compounding, 211 S. Bell Blvd, Cedar Park, TX 78613
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0047-2015·2014-11-05

    CVS Pain Relieving Antiseptic Spray Recalled for Microbial Contamination

    Wisconsin Pharmacal Company is recalling CVS Pharmacy Pain Relieving Antiseptic Spray because testing revealed microbial growth in the product.

    Product
    CVS pharmacy, Pain Relieving Antiseptic Spray. Benzalkonium Cl 0.13% Lidocaine HCl 2.5% 5 FL OZ (148 mL), OTC, Distributed by CVS Pharmacy, Inc., Woonsocket RI 02895 NDC 68093-6150-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0006-2015·2014-10-15

    Janssen Recalls Xarelto Tablets Due to Microbial Contamination

    Janssen Ortho L.L.C. is recalling 13,500 bottles of Xarelto (rivaroxaban) 15 mg tablets due to confirmed microbial contamination in a sales sample.

    Product
    Xarelto (rivaroxaban) Tablets 15 mg per tablet, 5 count bottle, Rx Only, Manufactured by: JOLLC, Gurabo, PR 00778 NDC 50458-578-99
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1560-2014·2014-09-03

    Central Admixture Recalls del Nido Cardioplegia Due to Microbial Contamination

    Central Admixture Pharmacy Services is recalling del Nido Cardioplegia with Lidocaine due to non-sterility and Aspergillus contamination.

    Product
    del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1562-2014·2014-09-03

    Central Admixture Pharmacy Recalls Contaminated Low Potassium Cardioplegia

    Central Admixture Pharmacy Services is recalling Low Potassium Cardioplegia doses due to non-sterility and Aspergillus contamination.

    Product
    LOW Potassium Cardioplegia 792 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1559-2014·2014-09-03

    Pediatric Cardioplegia Recalled for Aspergillus Microbial Contamination

    Central Admixture Pharmacy Services is recalling Pediatric Cardioplegia due to non-sterility and Aspergillus contamination. The product was distributed in Michigan and Wisconsin.

    Product
    PEDIATRIC CARDIOPLEGIA, 255 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1561-2014·2014-09-03

    Adenosine Injection Recalled for Microbial Contamination

    Central Admixture Pharmacy Services is recalling adenosine 90 mg injections in Michigan and Wisconsin due to Aspergillus species contamination.

    Product
    adenosine 90 mg in 0.9% sodium chloride/90 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1518-2014·2014-08-13

    Alcohol-Free Hand Sanitizer Recalled for Microbial Contamination

    HLI dba Humphreyline Inc is recalling 975 bottles of alcohol-free hand sanitizer due to microbial contamination. The product was distributed in Kentucky, Maryland, and Virginia.

    Product
    Alcohol-Free Hand Sanitizer, 1. fl. oz. (30 ml) bottles capped with white sprayer, OTC, contains Benzalkonium chloride. Mfg. for HLI, Portland, OR 97222 NDC: 19392-120-03. Labeled A) Anne Arundel County Mental Health Agency, Inc., B) Family Advocacy Program, and C) Henderson Com
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1497-2014·2014-08-06

    Fagron Recalls Pentravan Base Due to Mold Contamination

    Fagron is recalling six lots of Pentravan Base 2.5 Kg due to the presence of mold. The product is used for prescription compounding.

    Product
    Fagron, Pentravan Base 2.5 Kg, Article number: 802486. RX only, For prescription compounding, Oil-in-water emulsion, PLO gel alternative, Preserved and fragrance-free, Manufactured by; Fagron, Inc. 2400 Pilot Knob Rd, St. Paul, MN 55120 NDC 51552-0919-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1498-2014·2014-08-06

    Fagron Recalls Pentravan Plus Base Due to Mold Contamination

    Fagron is recalling specific lots of Pentravan Plus Base, a prescription compounding ingredient, because of mold contamination.

    Product
    Fagron, Pentravan Plus Base 2.5 Kg, Article number: 804749. RX only, For prescription compounding, Oil-in-water emulsion base alternative to PLO gel, Added emulsifier ad viscosity-enhancing agent for use with high concentrations of active ingredients.Pre served and fragrance-fr
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1496-2014·2014-08-06

    Fagron Recalls Phytobase Cream Lots Due to Mold Contamination

    Fagron is recalling six lots of Phytobase Cream, a prescription compounding vehicle, due to the presence of mold.

    Product
    Fagron, Phytobase Cream, 500 g, Article number: 802156. RX only, For prescription compounding Natural self-emulsifying oil-in water vehicle for oil-solvents ingredients. Contains Phytosomes (Plant Oil Bodies), Manufactured by Fagron, Inc. 2400 Pilot Knob Rd, St Paul, MN 55120,
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2112-2014·2014-08-06

    Wellspring Recalls IPM Wound Gel Rx Wound Dressing Due to Microbial Contamination

    Wellspring Pharmaceutical is recalling IPM Wound Gel Rx Wound Dressing due to a potential for microbial contamination. The product is distributed in the US and Canada.

    Product
    IPM Wound Gel Rx Wound Dressing IPM Wound Gel is indicated for the management of wound healing.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Food)·F-1954-2014·2014-05-28

    Stonyfield YoBaby Organic Yogurt Recalled for Elevated Coliform Levels

    Stonyfield Farm is recalling specific lots of YoBaby Pear/Peach Organic Whole Milk Yogurt due to elevated levels of coliforms.

    Product
    Stonyfield YoBaby Pear/Peach Organic Whole Milk Yogurt multipack- 6 pack plastic cups- 3 peach and 3 pear/4 oz each cups UPC-052159701161
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Drugs)·D-1213-2014·2014-04-16

    Zions RX Formulations Recalls Calcium Gluconate Injection Due to Contamination

    Zions RX Formulations is recalling 450 vials of Calcium Gluconate 10% for Injection due to a report of microbial contamination.

    Product
    Calcium Gluconate 10% for Injection, SDV 100 mL SDV, PF, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ, 85205.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1146-2014·2014-03-12

    Dr. Reddy's Recalls Lansoprazole Capsules Due to Microbial Contamination

    Dr. Reddy's is recalling multiple brands of Lansoprazole Delayed Release Capsules due to out-of-specification microbial counts.

    Product
    a) Walgreens Lansoprazole Delayed Release Capsules, USP 15 mg/Acid Reducer, 14 capsules per Bottle, Dist by Walgreen Company, 200 Wilmot RD Deerfield IL 60015 b) Family Wellness Lansoprazole Delayed Release Capsules, USP 15 mg/Acid Reducer, 14 capsules per Bottle, Distributed by
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1112-2014·2014-03-05

    Remel Recalls Oxoid Legionella BCYE Growth Supplement Due to Contamination

    Remel Inc is recalling specific lots of Oxoid Legionella BCYE Growth Supplement because the product may contain high levels of microbial contamination.

    Product
    Oxoid Legionella BCYE Growth Supplement, For 500 ml of medium, SR0110C, packaged 10 vials/box, lyophilized. The firm name on the label is Oxoid Ltd., Basingstoke, Hants, England. The product is used for the isolation of Legionella species from clinical and environmental samp
    Category
    Medical Device
    Distribution
    7 states