The Recall Desk

Hazard

Microbial Contamination recalls

1,324 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,324
Critical
313
Severe
678
Most recent
2026-10-21

Of the 1,324 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 678 (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.

976–1000 of 1324

  • ModerateFDA (Food)·F-2073-2016·2016-09-14

    Nature Made Hair Skin Nails Gummies Recalled for Microbial Count

    Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.

    Product
    Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1617-2016·2016-07-13

    Zarbee's Baby Omega 3 Liquid Supplement Recalled for Contaminants

    Zarbee's Naturals is recalling Baby Omega 3 liquid supplements because some units contain elevated aerobic plate counts and do not meet visual appearance standards.

    Product
    Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1618-2016·2016-07-13

    Zarbee's Recalls Baby Vitamin D Liquid Due to Contaminants

    Zarbee's Naturals is recalling specific lots of Baby Vitamin D liquid supplements because some units contain elevated aerobic plate counts and do not meet visual appearance standards.

    Product
    Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0853-2016·2016-05-25

    Keystone Recalls Better Braid Un-Braid Due to Microbial Contamination

    Keystone Laboratories is recalling Better Braid Un-Braid salicylic acid product due to a failed S. aureus test. The product was distributed in Maryland and New Jersey.

    Product
    BETTER BRAIDS UN-BRAID (salicylic acid), Le Demelant, Packaged in 12 FL. OZ. (355 ml) Bottles, Over the Counter Only. Distributed by KEYSTONE LABORATORIES, UPC 07059600430.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-1250-2016·2016-05-04

    Tarry Medical Recalls DandleLION Kisses Due to Microbial Contamination

    Tarry Medical Products is recalling DandleLION Kisses sterile sucrose solution due to microbial contamination. The product is distributed in nine states.

    Product
    DandleLION Kisses, 24% Sterile Organic Sucrose In Purified Water, 2 ml polyethylene vial. For oral use Part Number D 12442 C384
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0726-2016·2016-03-02

    Keystone Recalls Medicated Better Braids Spray Due to Staphylococcus aureus

    Keystone Laboratories is recalling Medicated Better Braids, La Laque (salicylic acid) Spray due to a positive Staphylococcus aureus test result.

    Product
    Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0655-2016·2016-02-17

    Fagron Recalls SyrSpend SF Grape Flavor Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0656-2016·2016-02-17

    Fagron Recalls SyrSpend SF Suspending Base Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0654-2016·2016-02-17

    Fagron Recalls SyrSpend SF Syrup Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF syrup-suspending vehicle due to the presence of yeast. The recall affects 44 bottles distributed nationwide.

    Product
    SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2016·2016-02-10

    MediChoice Cohesive Bandages Recalled for Microbial Contamination

    Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination.

    Product
    MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2016·2016-02-10

    Owens & Minor Recalls MediChoice Cohesive Bandages Due to Microbial Contamination

    Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination. The affected bandages were distributed nationwide.

    Product
    MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2016·2016-02-10

    Owens & Minor Recalls MediChoice Cohesive Bandages Due to Microbial Contamination

    Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination. The affected products were distributed nationwide.

    Product
    MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging]. General Hospital Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0577-2016·2016-01-27

    Energique Joint Pain Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique Joint Pain & Stiffness Relief Topical Spray due to microbial contamination. Testing revealed out-of-specification results for total aerobic microbiological count.

    Product
    Energique, Homeopathic Remedy, Joint Pain & Stiffness Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0133-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Joint Pain & Stiffness Relief, Topical Homeopathic Spray, NDC 50845-0218-1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0575-2016·2016-01-27

    FDA Recalls Energique Homeopathic Skin Spray Due to Microbial Contamination

    Grato Holdings, Inc. is recalling 118 bottles of Energique homeopathic skin spray due to out-of-specification microbial counts.

    Product
    Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bottle, NDC 44911-0136-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Skin Irritant & Healing Support, Topical Homeopathic Spray, NDC 50845-0214-1, Dist…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0580-2016·2016-01-27

    FDA Recalls Energique Homeopathic Pain Spray for Microbial Contamination

    Grato Holdings is recalling Energique First Aid Pain & Trauma Relief homeopathic spray due to out-of-specification microbial counts.

    Product
    Energique, Homeopathic Remedy, First Aid Pain & Trauma Relief, 1 fl oz (30 ml) bottles, NDC 44911-0135-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, First Aid Pain & Trauma Relief, Topical Homeopathic Spray, NDC 50845-0216-1, Dist By…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0578-2016·2016-01-27

    Grato Holdings Recalls Energique Shingles Pain Spray Due to Microbial Contamination

    Grato Holdings is recalling Energique Shingles Pain & Ulceration Relief Topical Spray due to out-of-specification microbial counts. The recall covers 371 bottles distributed nationwide and to Guatemala and Canada.

    Product
    Energique, Homeopathic Remedy, Shingles Pain & Ulceration Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0137-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Shingles Pain & Ulceration Relief Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0576-2016·2016-01-27

    Energique Homeopathic Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique homeopathic topical spray due to out-of-specification microbial counts. The product was distributed nationwide and to Canada and Guatemala.

    Product
    Energique, Homeopathic Remedy, Muscle/Tendon Pain & Stress Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0132-1, Dist. by Energique, Inc. Woodbine, IA 51579; ALSO LABELED AS --- Liddell Laboratories, Muscle/Tendon Pain & Stress Relief, Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0579-2016·2016-01-27

    Energique Headache Spray Recalled for Microbial Contamination

    Grato Holdings is recalling Energique Headache Pain & Sinus Pressure Relief Topical Spray due to microbial contamination.

    Product
    Energique, Homeopathic Remedy, Headache Pain & Sinus Pressure Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0134-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Headache Pain & Sinus Pressure Relief, Topical Homeopathic Spray, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3068-2015·2015-09-09

    HoneyCombs Formula C&F Recalled for Excessive Coliform Bacteria

    HoneyCombs Industries is recalling 161 bottles of Formula C&F droppers because the powdered golden seal ingredient contained coliform bacteria levels exceeding specifications.

    Product
    Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3069-2015·2015-09-09

    HoneyCombs Formula IM Recalled for Excessive Coliform Bacteria

    HoneyCombs Industries is recalling 55 bottles of Formula IM because the powdered golden seal ingredient contained coliform bacteria levels above the specified limit.

    Product
    Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2095-2015·2015-07-22

    Alere i Influenza A & B Kit Recalled for False Negative Risk

    Alere is recalling 257 kits of the Alere i Influenza A & B test due to microbial growth that may cause false negative results.

    Product
    Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on the Alere" i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1064-2015·2015-05-20

    Mission Pharmacal Recalls Sodium Sulfacetamide and Sulfur Wash Kits

    Mission Pharmacal is recalling 2,412 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.

    Product
    Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit, Rx Only, Sodium Sulfacetamide 9% and Sulfur 4.5% Wash, Net Wt. 16 oz (454 g), Daily Moisturizing Wash, 16 fl. oz. (473 mL), Manufactured for: BioComp Pharma Inc., San Antonio, TX 78230, NDC 44523-0609-23
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1065-2015·2015-05-20

    Mission Pharmacal Recalls Sodium Sulfacetamide and Sulfur Wash Kits

    Mission Pharmacal is recalling 1,992 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.

    Product
    Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen, Rx Only, Sunscreen Broad Spectrum SPF 25, Net Wt. 3 oz (85 g), Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Net Wt. 16 oz (454 g), Manufactured for: BioComp Pharma Inc., San Antonio TX, 78230, NDC 44523-616-23
    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…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-451-2015·2015-04-15

    Central Admixture Pharmacy Services Recalls TPN Bags Due to Sterility Failure

    Central Admixture Pharmacy Services is recalling 5 bags of Total Parenteral Nutrition (TPN) compounded for Walter Reed National Military Medical Center because sterility tests failed.

    Product
    Walter Reed Natl Mil Med Ctr (MD) Stock TPN D10% without Ca, Trophamine 12g, Dextrose 20g, compound vol: 200 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is lined with a polystyrene insert; CAPS, Allentown, PA.
    Category
    Drug
    Distribution
    Distributed nationwide