The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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26751–26775 of 39747

  • SevereFDA (Devices)·Z-2536-2015·2015-09-09

    MAHURKAR Acute Dialysis Catheters Recalled for Potential Sterility Compromise

    FDA is recalling MAHURKAR 12Fr Acute Dialysis Catheters due to a potential compromise in sterility.

    Product
    MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20cm, Curved Extensions, PASS Tray Item Code: 8888103003HP Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2534-2015·2015-09-09

    Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled for Sterility Concerns

    Covidien LLC is recalling 171 kits of Mahurkar Elite Acute Triple Lumen Catheter Trays because sterility may be compromised.

    Product
    Mahurkar Elite Acute Triple Lumen Catheter Tray, Curved Extensions with IC* Safety Components, 12.5 Fr x 20 cm Item Code: 8888233420 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3078-2015·2015-09-09

    Chetak Recalls Deep Coriander Powder Due to Salmonella Risk

    Chetak New York is recalling 300 jars of Deep Coriander Powder because they may be contaminated with Salmonella.

    Product
    Deep All Natural Spices Coriander Powder, Net Wt 400g/14.1 oz Product of India, Distributed by: Chetak New York, L.L.C. Edison, NJ 08837 USA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2537-2015·2015-09-09

    Recall of Mahurkar Acute Dialysis Catheters Due to Sterility Concerns

    Covidien LLC is recalling 550 kits of Mahurkar 12Fr Acute Dialysis Catheters because sterility may be compromised. The products were distributed nationwide.

    Product
    MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20cm, Straight Extensions, PASS Tray Item Code: 8888104003HP Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2535-2015·2015-09-09

    MAHURKAR Acute Dialysis Catheter Recalled for Potential Sterility Compromise

    Covidien LLC is recalling 569 MAHURKAR 12Fr Acute Dialysis Catheters because sterility may be compromised. The products were distributed nationwide in the US.

    Product
    MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16cm, Curved Extensions, PASS Tray Item Code: 8888103002HP Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3082-2015·2015-09-09

    Westbrook's Cannery Recalls Horseradish Dill Pickles Due to Underprocessing

    Westbrook's Cannery is recalling 16-ounce jars of Horseradish Dill Pickles because the products may be underprocessed. Consumers in 11 states should stop using the product.

    Product
    WESTBROOK'S CANNERY HORSERADISH DILL PICKLES, Net WT. 16 oz (453.592G) glass jars, Ingredients: Cucumbers, White Distilled Vinegar, Water, Pickling Salt, Horseradish, Garlic Cloves, Dill Seed, Dill Weed, Alum 221 West Third Street - Zoar, OH 44697 www.wesbrookscannery.com UPC 8…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-1409-2015·2015-09-09

    Estradiol and Estriol Capsules Recalled for Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling Estradiol and Estriol capsules due to potential penicillin cross-contamination. The affected products were distributed nationwide.

    Product
    Estradiol, Estriol capsules, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3064-2015·2015-09-09

    Good Seed Recalls Soybean and Mung Bean Sprouts for Listeria Risk

    Good Seed, Inc. is voluntarily recalling soybean and mung bean sprouts due to potential Listeria monocytogenes contamination.

    Product
    Soybean sprouts, 1, 2 & 10-lb clear plastic bags labeled GOODSEED Soy Bean Sprouts Keep Refrigerated
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2488-2015·2015-09-09

    Synthes Recalls VEPTR Inferior Cradles Due to Mechanical Failure Risk

    Synthes (USA) Products LLC is recalling VEPTR Inferior Cradles because a partially formed hole may cause mechanical failure, potentially requiring surgery.

    Product
    VEPTR Vertical Expandable Prosthetic Titanium Rib, inferior cradles also known as caudal rib supports. The VEPTR/VEPTR II devices mechanically stabilize and/or correct thoracic deformities to allow the chest and lungs to grow.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1415-2015·2015-09-09

    Bi-Est and Progesterone Vaginal Suppositories Recalled for Penicillin Contamination

    South Coast Specialty Compounding is recalling Bi-Est and Progesterone Vaginal Suppositories due to potential penicillin cross-contamination.

    Product
    Bi-Est (estriol,estradiol), Progesterone Vaginal Suppository, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1407-2015·2015-09-09

    South Coast Specialty Compounding Recalls Tri-Est 80:10:10 Capsules

    South Coast Specialty Compounding is recalling Tri-Est 80:10:10 capsules due to potential penicillin cross-contamination. The affected products were distributed nationwide.

    Product
    Tri-Est 80:10:10 Progesterone (estriol, estradiol, estrone, progesterone) capsules Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1410-2015·2015-09-09

    Bi-Est Hormone Drops Recalled for Potential Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling five prescriptions of Bi-Est hormone drops due to potential penicillin cross contamination.

    Product
    Bi-Est (estriol,estradiol), Progesterone, DHEA, Testosterone drops, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3081-2015·2015-09-09

    Westbrook's Dilly Beans Recalled for Potential Underprocessing

    Westbrook's Cannery is recalling 12-ounce jars of Dilly Beans because they may be underprocessed. The product was distributed to 11 states.

    Product
    West brook's Dilly Beans, Net WT. 12 oz (354.882g) glass jars, Ingredients: White Distilled Vinegar, Water, Green Beans, Alum, Pickling Salt, Spices 330-874-8120 www.wesbrookscannery.com UPC 8 53238 00440 7
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-2517-2015·2015-09-09

    Halyard Health Recalls KimVent Multi-Access Port Replacement Catheters

    Halyard Health is recalling KimVent Multi-Access Port Replacement Catheters because the thumb valve may remain partially open after suctioning, potentially compromising the closed suction system.

    Product
    KimVent* Multi-Access Port Replacement Catheter for Adults,Tracheostomy, 14 F (Product Code 2401453-5) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2710-2015·2015-09-09

    Customed Curations Kits Recalled Due to Sterilization Validation Issues

    Customed, Inc. is recalling Curations Kits in Puerto Rico because the sterilization process and package integrity were not adequately validated.

    Product
    CURATION KIT 10/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2684-2015·2015-09-09

    Customed Surgical Gowns Recalled for Sterilization Validation Deficiencies

    Customed, Inc. is recalling surgical gowns due to inadequate validation of sterilization processes and package integrity. The products were distributed only in Puerto Rico.

    Product
    SURG GOWN POLYREINF LGE CUSTOM 28/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2526-2015·2015-09-09

    Mahurkar Acute Dual Lumen Catheter Tray Recalled for Sterility Concerns

    Covidien LLC is recalling 96 kits of Mahurkar Acute Dual Lumen Catheter Trays because sterility may be compromised.

    Product
    Mahurkar Acute Dual Lumen Catheter Tray, High Flow Straight Extensions with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135137 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1337-2015·2015-09-09

    Bi-Est 80:20 Progesterone Capsules Recalled for Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling Bi-Est 80:20 Progesterone capsules due to potential penicillin cross-contamination.

    Product
    Bi-Est 80:20 Progesterone (estriol,estradiol, progesterone) capsules, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2589-2015·2015-09-09

    Customed D & C Laparoscopy Packs Recalled for Sterilization Defects

    Customed, Inc. is recalling 192 D & C Laparoscopy Packs distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.

    Product
    D & C LAPAROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1342-2015·2015-09-09

    Methyl Folate Injection Recalled Due to Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling Methyl Folate Injection vials due to potential penicillin cross-contamination. The recall covers 335 vials distributed nationwide.

    Product
    Methyl Folate Lyophilized Powder for Injection, 20 mg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1339-2015·2015-09-09

    Meloxicam Capsules Recalled for Potential Penicillin Cross Contamination

    South Coast Specialty Compounding is recalling Meloxicam 12 mg capsules due to potential penicillin cross contamination. The recall covers all lots expiring in August 2015.

    Product
    Meloxicam capsules, 12 mg, Rx Only, Manufactured by Park Compounding, Irving, CA -non-sterile formulation
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2692-2015·2015-09-09

    Customed Recalls Laparoscopy-Gyn Surgical Packs Due to Sterilization Issues

    Customed, Inc. is recalling 84 units of Laparoscopy-Gyn Surgical Packs distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.

    Product
    LAPAROSCOPY-GYN SURGICAL PACK Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2615-2015·2015-09-09

    Customed Endoveneous Custom Packs Recalled for Sterilization Validation Issues

    Customed, Inc. is recalling 20 units of Endoveneous Custom Packs in Puerto Rico due to inadequate validation of sterilization processes and package integrity.

    Product
    ENDOVENOUS CUSTOM PACK 5/CS CUSTOMED Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
    Category
    Medical Device
    Distribution
    1 state