The Recall Desk

Hazard

Contamination recalls

2,060 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,060
Critical
83
Severe
615
Most recent
2026-09-09

Of the 2,060 contamination recalls we have scored against our rubric, 83 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 615 (30%) 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 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.

1226–1250 of 2060

  • SevereFDA (Food)·F-0652-2016·2016-03-09

    Dole Recalls Salads from Springfield Ohio Facility Due to Operational Suspension

    Dole Fresh Vegetables Inc is withdrawing all salads produced at its Springfield, Ohio facility, including Dole and private label brands, due to a suspension of operations.

    Product
    Colorful Coleslaw Display, 2 lb. bag - Sam's Club; Colorful Coleslaw - 14 oz. bag- Dole All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0676-2016·2016-03-09

    Dole Recalls Arugula and Salads from Springfield, Ohio Facility

    Dole is withdrawing all Dole and private label salads produced in Springfield, Ohio, to suspend operations at the facility.

    Product
    Arugula, 5 oz. clamshell, Dole brand. . All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0688-2016·2016-03-09

    Dole Recalls Cole Slaw and Salads from Springfield Facility

    Dole is withdrawing all Dole and private label salads produced in Springfield, OH, to suspend operations at the facility.

    Product
    Cole Slaw with Carrots Separate, 5 lb. bag, Dole brand. All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0665-2016·2016-03-09

    Dole Recalls Salads from Springfield Facility Due to Operational Suspension

    Dole is withdrawing all salads produced in Springfield, OH, including Kroger and Dole brands, as the company suspends operations at the facility.

    Product
    Veggie Blend, 12 oz. bag - Kroger; Very Veggie, 12 oz. bag - Dole All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0644-2016·2016-03-09

    Dole Recalls Caesar Salad Kits from Springfield Ohio Facility

    Dole is withdrawing Caesar salad kits produced in Springfield, Ohio, due to a facility suspension.

    Product
    Caesar Kit, 10 oz. bag, - Aldi; Dole 14.53 oz bag, 22.30 oz. - Walmart; Value Size All Natural Caesar Kit , 15 oz. bag - Dole All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2016·2016-03-09

    Cook Inc. Recalls Kopans Breast Lesion Localization Needles

    Cook Inc. is recalling 134 Kopans Breast Lesion Localization Needles because they may have been exposed to body fluids during processing, posing a potential risk of blood-borne pathogen transmission.

    Product
    Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle with centimeter markings and a hookwire. The hookwire features a burnish mark that allows the operator to ensure that the hookwire is within the needle tip during
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0666-2016·2016-02-24

    Alcon Recalls TEARS Naturale FREE Eye Drops Due to Sterility Concerns

    Alcon is recalling TEARS Naturale FREE eye drops because some vials may contain water instead of the product, creating a sterility risk.

    Product
    TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops, 1% and 0.3%, Preservative Free, 0.9 mL (0.03 FL OZ) Single-Use Vials, packaged in 60-count Single-Use Vials per carton, Manufactured for: Alcon Laboratories, Inc., Fort Work, TX 76134, Barcode 9001674110
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0361-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Coho Salmon Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of smoked coho salmon due to potential Clostridium botulinum contamination.

    Product
    Smoked Coho (salmon), Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67222 3
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0365-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Jalapeno Spring Chinook Salmon Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of smoked jalapeno spring Chinook salmon due to potential Clostridium botulinum contamination.

    Product
    Smoked Jalapeno Spring Chinook (salmon), Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67392 3
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0623-2016·2016-01-20

    ArthroCare Cavity 8 Gauge Spine Wand Recalled for Sterile Barrier Failure

    ArthroCare Corporation is recalling 262 Cavity 8 Gauge Spine Wands because cracking in the tray compromises the sterile barrier.

    Product
    Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0606-2016·2016-01-13

    Baxter INTERLINK Y-Type Solution Set Recalled for Particulate Matter

    Baxter Healthcare is recalling INTERLINK Y-Type Solution Sets due to potential dark particulate matter on the spike adapter.

    Product
    Baxter INTERLINK System, Y-Type Solution Set, 78 (2.0 m), 2 Injection Sites, Male Luer Lock Adapter, 1C8581 s, Product Usage: C8581: For the administration of fluids from a container into the patients vascular system through a vascular access device. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0435-2016·2015-12-30

    Salted Smoked Split Herring Recalled for Being Uneviscerated

    P East Trading Corporation is recalling salted smoked split herring in bulk wooden boxes because the product was found to be uneviscerated.

    Product
    Salted Smoked Split Herring in bulk wooden boxes, Net Wt. 18 lbs., Product of Canada --- No label provided for bulk product.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0470-2016·2015-12-30

    Hardy Diagnostics Recalls FB Broth Due to Potential Contamination

    Hardy Diagnostics is recalling FB Broth (Lot 15231) because of potential Burkholderia fungorum contamination. The product was distributed in California, Wisconsin, Maryland, and Utah.

    Product
    FB Broth, 10ml (Fastidious Bacteria Broth) Cat. no: K31 Lot: 15231 A fastidious bacteria broth for the enriched cultivation of Neisseria spp., Haemophilus spp., Streptococcus spp., Corynebacterium spp., and other fastidious bacteria from clinical specimens.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Drugs)·D-0490-2016·2015-12-09

    Life Science Pharmacy Recalls Compounded Estriol Vaginal Creams

    Life Science Pharmacy Inc. is recalling compounded Estriol Vaginal Creams due to potential penicillin cross-contamination.

    Product
    ESTRIOL Vaginal Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0334-2016·2015-12-02

    BD CD64 APC-R700 Reagent Recalled Due to CD4 Antibody Contamination

    Becton, Dickinson and Company is recalling three lots of CD64 APC-R700 reagent because they are contaminated with CD4 antibody, which may cause unexpected staining patterns.

    Product
    BD CD64 APC-R700; Analyte Specific Reagent; Model 657701; Lot No. 4344945, 5037611 and 5063945. Hematology - used as analyte specific reagent - contamination leads to possibility of unexpected staining pattern.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0237-2016·2015-11-25

    US Compounding Recalls Alprostadil Vials Due to Sterility Assurance Concerns

    US Compounding Inc is recalling 82 vials of Alprostadil (PGE-1) nationwide due to deficient practices that may impact sterility assurance.

    Product
    Alprostadil (PGE-1), 5 mL (40 mcg/mL) in 10 mL Multi-Dose Vial, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC: 62295-3253-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0297-2016·2015-11-25

    Roche Bulk Loader Module Recalled for Sample Contamination Risk

    Roche Diagnostics is recalling Bulk Loader Modules for cobas p 512/612 instruments because sample tubes may open during transport, causing system and sample contamination.

    Product
    Bulk Loader Module for cobas p 512/612 Pre-analytical sample handling that includes de-capping, aliquoting and sorting of samples for analysis. In vitro diagnostic machine component.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-0213-2016·2015-11-18

    The Compounder Recalls Hormone Capsules Due to Penicillin Cross-Contamination

    The Compounder is recalling specific lots of compounded hormone capsules because an active ingredient was contaminated with penicillin.

    Product
    E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) : TESTOST (Testosterone USP) IN OLIVE OIL 0.75 : 3 : 50 : 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0268-2016·2015-11-18

    Medtronic Perfusion Tubing Packs Recalled for Potential Header Bag Seal Breach

    Medtronic is recalling 496 Perfusion Tubing Packs due to a potential breach in the header bag seal. The affected lots were distributed nationwide in the US.

    Product
    Medtronic Perfusion Tubing Packs, Models TL7M64R3, TL7P17R1 & HY2W85R9, Sterilized using Ethylene Oxide. The Tubing Pack design and components are specified by the user, they are packaged with consideration of setup efficiency and respect for the environment, and they are inte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0135-2016·2015-11-04

    Moses Lake Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns

    JD & SN Inc. is recalling 50 mg testosterone pellets because the FDA cannot ensure the sterile compounded drugs are free from contamination.

    Product
    TESTOSTERONE, Pellet, 50 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0100-2016·2015-11-04

    Moses Lake Pharmacy Recalls Hydroxyprogesterone Caproate Oil Due to Sterility Concerns

    JD & SN Inc. is recalling specific syringes of Hydroxyprogesterone Caproate Oil because the FDA cannot ensure the sterile compounded drugs are free from contamination.

    Product
    HYDROXYPROGESTERONE CAPROATE OIL, injectable Solution, 250 mg/mL, syringe sizes: 4 mL; 5 mL; 6 mL; 10 mL; 16 mL; 18 mL; 20 mL; and 22 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1823-2015·2015-09-30

    PharMEDium Recalls Bupivacaine Bags Due to Human Hair Particulate Matter

    PharMEDium Services is recalling 20 bags of Bupivacaine HCl 0.0625% for epidural use because they contain human hair particulate matter.

    Product
    Bupivacaine HCl 0.0625%, 250 mL total volume in a 250 mL LifeCare Bag in Sodium chloride 0.9%, Epidural Use Only, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-197-50
    Category
    Drug
    Distribution
    Distributed nationwide