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.

1251–1275 of 2060

  • SevereFDA (Drugs)·D-1824-2015·2015-09-30

    PharMEDium Recalls Morphine Sulfate IV Bags Due to Particulate Matter

    PharMEDium Services is recalling 100 bags of Morphine Sulfate IV solution because the sodium chloride used contained human hair.

    Product
    Morphine Sulfate, 1 mg per mL (250 mg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-181-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1828-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Bags Due to Particulate Matter

    Pharmedium Services is recalling 120 bags of Phenylephrine HCl injection due to the presence of human hair particulate matter.

    Product
    PHENYLephrine HCl, 10 mg added to 250 mL 0.9% Sodium Chloride Injection USP (40 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-149-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1825-2015·2015-09-30

    PharMEDium Recalls Fentanyl Citrate IV Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 663 bags of Fentanyl Citrate IV solution because the sodium chloride used contained human hair.

    Product
    Fentanyl Citrate, 5 mcg per mL (1,250 mcg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-107-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1821-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Due to Human Hair Contamination

    Pharmedium Services, LLC is recalling specific lots of Phenylephrine HCl injection because the sodium chloride base used contained human hair.

    Product
    PHENYLephrine HCl, 50 mg added to 250 mL 0.9% Sodium Chloride Injection USP (200 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-171-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1827-2015·2015-09-30

    Pharmedium Phenylephrine Injection Recalled for Particulate Matter

    Pharmedium Services, LLC is recalling 48 bags of Phenylephrine HCl injection due to the presence of particulate matter, specifically human hair, in the product.

    Product
    PHENYLephrine HCl, 60 mg added to 250 mL 0.9% Sodium Chloride Injection USP (240 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-236-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1822-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter

    Pharmedium Services is recalling specific lots of Phenylephrine HCl injection due to the presence of human hair particulate matter.

    Product
    PHENYLephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection USP (160 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-169-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2748-2015·2015-09-16

    Elcam Medical stopcock recall due to punctured blister packages

    Elcam Medical is recalling stopcocks because punctured blister packages were found during manufacturing, creating a potential for device contamination.

    Product
    Elcam Medical Minimal Residual Volume Luer activated Swabbable stopcock (MRVLS) for pressure monitoring and intravenous fluid administration; Manufactured by: Elcam Medical ACAL, Israel. Sterile, Quantity 20.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2749-2015·2015-09-16

    Elcam Medical MANI 3G Plate BLS RAD B.BRAUN Recalled for Punctured Packaging

    Elcam Medical is recalling MANI 3G Plate BLS RAD B.BRAUN manifolds because punctured blister packages were detected during manufacturing, creating a potential for device contamination.

    Product
    Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring and intravenous fluid administration. Manufactured by: Elcam Medical ACAL, Israel; Distributed by: Elcam Medical Inc., USA. Sterile
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Drugs)·D-1413-2015·2015-09-09

    Estradiol Cream Recalled for Potential Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling 24 prescriptions of Estradiol cream due to potential penicillin cross contamination.

    Product
    Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2524-2015·2015-09-09

    Stryker Neptune 2 Waste Management System Docking Station Recall

    Stryker is recalling Neptune 2 Waste Management System Docking Stations because a defective component may cause fluid leaks during use.

    Product
    Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker Docking Station (Docker) is a component of the Neptune 2 Waste Management System. The Stryker Rover, another component of the system, is a mobile unit used to suc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1351-2015·2015-09-02

    Teva Recalls ADRUCIL Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals USA is recalling ADRUCIL (fluorouracil injection) vials due to the presence of silicone rubber and fluorouracil crystals in the solution.

    Product
    ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by Teva Parenteral Medicines, Inc., Irvine, CA. NDC 073-3019-11 (individual vial), NDC 0703-3019-12 (carton of five).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3042-2015·2015-08-26

    Natar Foods Recalls Uneviscerated Dry Bream Fish

    Natar Foods, Inc. is recalling vacuum-packed dry bream fish found to be uneviscerated. The product was distributed in seven states.

    Product
    Dry Bream-lesh (Fish), Net Wt. varies - weighed upon sale, product is vacuum packed, Distributed by: Royal Sweet Bakery 119 49 Street Brooklyn, NY 11232, PRODUCT OF RUSSIA
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-1349-2015·2015-08-26

    Bausch & Lomb Recalls Bromfenac Ophthalmic Solution Due to Sterility Concerns

    Bausch & Lomb is recalling 13,995 bottles of Bromfenac Ophthalmic Solution, 0.09%, because preservative testing failed, raising concerns about sterility.

    Product
    Bromfenac Ophthalmic Solution, 0.09%, 1.7 mL Bottle, Rx Only. Manufactured by Bausch & Lomb Incorporated Tampa, FL 33637. NDC: 24208-439-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2384-2015·2015-08-26

    C.R. Bard Recalls Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters

    C.R. Bard is recalling 14,310 units of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.

    Product
    Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2417-2015·2015-08-26

    Radiometer Fixation Kit N20 Recalled for Paper Coating Transfer

    Radiometer America Inc is recalling Fixation Kit N20 units because paper liner coating may stick to the fixation ring.

    Product
    Radiometer Fixation Kit N20 for the TCM CombiM monitoring system, REF 905-873. The Fixation Kit N20 is used to apply tc Sensor 84 and tc Sensor 54 on the skin of a patient. TC sensor 84 and 54 are used with the TCM CombiM monitoring system and the Philips TcG10 module. The T
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2382-2015·2015-08-19

    B. Braun Recalls Celsite Implantable Access Port Systems Due to Endotoxin

    B. Braun Interventional Systems is recalling 11 Celsite Implantable Access Port Systems because endotoxin test results were out of specification.

    Product
    Celsite Implantable Access Port System, model ST301. The Celsite Implantable Access Port Systems (Celsite port systems) are implantable port and catheter systems that allow safe, repeated access to the patient's bloodstream. The port chamber and catheter design can be used for
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2118-2015·2015-07-29

    FDA Recalls Non-Sterile Subassemblies Due to Sterility Compromise

    FDA is recalling specific non-sterile subassemblies from Covidien LLC because they contain splits or holes that compromise sterility.

    Product
    Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE SUBASSEMBLY SA1578 NO-STERILE SUBASSEMBLY SA2000 NON STERILE SUBASSEMBLY SA2001 NON STERILE SUBASSEMBLY SA2002 NON STERILE SUBASSEMBLY SA2004 NON STERILE SUBASSEMBLY SA2005 NON STERILE SUBASSEMBLY SA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2182-2015·2015-07-29

    FDA Recalls Fiber Stripper Tools Due to Cleaning Validation Issues

    American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.

    Product
    Tool, Stripper W/BLD, 28S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes, corresp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1240-2015·2015-07-22

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira is recalling 314,600 bags of 0.9% Sodium Chloride Injection USP due to potential channel leaks that may compromise sterility.

    Product
    0.9% Sodium Chloride Injection USP, 50 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira, Inc., Ausitn, TX 78728, NDC 00409-7101-68
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1181-2015·2015-07-08

    Lincare Recalls Vancomycin Syringes Due to Sterility Assurance Concerns

    Lincare, Inc. is recalling Vancomycin HCL 250mg syringes compounded by United Medical IV Center in Arkansas because the sterility of the product is not assured.

    Product
    VANCOMYCIN HCL 250mg / NS 6mL syringe, Packaged in 6 mL Syringes, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1171-2015·2015-07-08

    Lincare Recalls Vancomycin IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling Vancomycin IV bags compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    VANCOMYCIN 1.25gm / NS 250mL AccuFlo, Qty: 7 250 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1196-2015·2015-07-08

    Lincare Recalls Vancomycin Bags Due to Sterility Assurance Concerns

    Lincare, Inc. is recalling 2 bags of Vancomycin 750 mg/NS 100 ml compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    Vancomycin 750 mg/NS 100 ml accuflo, Packaged in 100 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1953-2015·2015-07-08

    Sheffield Pharmaceuticals Recalls LUBRI GEL Due to B. cepacia Contamination

    Sheffield Pharmaceuticals is recalling specific lots of Dr. Sheffield's LUBRI GEL personal lubricant after testing revealed high counts of gram-positive rods and B. cepacia.

    Product
    Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant.
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Drugs)·D-1122-2015·2015-06-17

    Montana Compounding Pharmacy Recalls Glutathione Nasal Solution Due to Sterility Concerns

    Montana Compounding Pharmacy is recalling specific lots of Glutathione Nasal Solution because FDA inspectors observed objectionable conditions that raise concerns about the product's sterility.

    Product
    Glutathione INHALATION (PF), NASAL solution, 100 mg/mL, 3 mL vial, Rx only, dispensed by Montana Compounding Pharmacy, Missoula, MT
    Category
    Drug
    Distribution
    2 states