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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26776–26800 of 39747

  • SevereFDA (Devices)·Z-2688-2015·2015-09-09

    Customed Recalls Lap-Cholecystectomy Surgical Packs Due to Sterilization Issues

    Customed, Inc. is recalling 320 lap-cholecystectomy surgical packs distributed in Puerto Rico because of inadequate validation of sterilization processes and package integrity.

    Product
    LAP-CHOLECYSTECTOMY 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-2533-2015·2015-09-09

    Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled for Sterility Concerns

    Covidien LLC is recalling 165 Mahurkar Elite Acute Triple Lumen Catheter Trays because sterility may be compromised. The affected units were distributed nationwide.

    Product
    Mahurkar Elite Acute Triple Lumen Catheter Tray, Curved Extensions with IC* Safety Components, 12.5 Fr x 13 cm Item Code: 8888233413 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1411-2015·2015-09-09

    FDA Recalls Estriol and Estradiol Cream Due to Penicillin Contamination

    South Coast Specialty Compounding is recalling 61 prescriptions of Estriol and Estradiol cream because the products may be contaminated with penicillin.

    Product
    Estriol,Estradiol cream, Rx only, Manufactured by Park Compounding, Irvine, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1341-2015·2015-09-09

    FDA Recalls Chorionic Gonadotropin Injectable Due to Penicillin Contamination

    South Coast Specialty Compounding is recalling Chorionic Gonadotropin/Hydroxocobalamin Injectable vials due to potential penicillin cross-contamination.

    Product
    Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2494-2015·2015-09-09

    Halyard KimVent Closed Suction System Thumb Valve Recall

    Halyard Health is recalling KimVent Closed Suction Systems because the thumb valve may remain partially open after suctioning, despite appearing locked.

    Product
    KimVent* Wet Pak* Closed Suction System for Adults, 14 F, DT, T-Piece (Product Code 220569) 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 airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2538-2015·2015-09-09

    Panoramic X-ray Model PC-1000 Recalled for Jackscrew Nut Failure

    Panoramic Rental Corp. is recalling 7,885 Panoramic X-ray Model PC-1000 units due to a jackscrew nut part failure that could cause device malfunction and injury.

    Product
    Panoramic X-ray Model PC-1000 The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser 1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2015·2015-09-08

    Olli Salumeria Americana Recalls Pork Salami Due to Misbranding

    Olli Salumeria Americana is recalling pork salami products because the packaging lacks an ingredient list, failing to disclose the presence of sulfites from wine.

    Product
    OLLI SALUMERIA AMERICANA — Olli Salumeria Americana, LLC Recalls Pork Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·121-2015·2015-09-08

    Schrader Farms Recalls Ground Beef Due To Possible Non-O157 E. Coli Contamination

    Schrader Farms is recalling approximately 20 pounds of ground beef sold in Seneca County, New York, due to possible non-O157 E. coli contamination.

    Product
    Schrader Farms, LLC — Schrader Farms Meat Market Recalls Beef Product Due To Possible Non-O157 E. Coli Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E073000·2015-09-08

    Cummins Recalls ISB, ISL, and ISX Engines Due to Stalling Risk

    Cummins is recalling certain ISB6.7, ISL9, ISX12, and ISX15 engines because a faulty Engine Control Module may cause the engine to stall without warning, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:IGNITION:MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V562000·2015-09-04

    New Flyer Transit Buses Recalled for Potential Steering Loss

    New Flyer is recalling 432 transit buses from 2013-2015 because a tie rod clamp may be improperly torqued, risking a loss of steering.

    Product
    NEW FLYER — NEW FLYER XN40, XN35, XD40, XD60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V561000·2015-09-04

    Keystone Recalls 2008-2009 Travel Trailers Due to Fire Risk

    Keystone is recalling 2008-2009 travel trailers and fifth wheels because a transfer switch may overheat and cause a fire.

    Product
    KEYSTONE — KEYSTONE CHALLENGER, RAPTOR, BIG SKY, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V557000·2015-09-03

    Fontaine Recalls 2015 Traverse HT Trailers Due to Suspension Defect

    Fontaine Trailer Company is recalling 2015 Traverse HT trailers because a suspension member may separate from the trailer, increasing the risk of a crash.

    Product
    FONTAINE — FONTAINE TRAVERSE HT
    Category
    Vehicle
    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
  • CriticalFDA (Food)·F-3047-2015·2015-09-02

    Fisher Brand Chopped Walnuts Recalled Due to Salmonella Contamination

    John B. Sanfilippo & Son Inc. is recalling Fisher Brand chopped walnuts after FDA testing found Salmonella. Consumers should stop using the product.

    Product
    Fisher Brand chopped walnuts, packaged in 10 ounce, polyethylene stand-up bag with zipper. The bag is blue with white lettering.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-3045-2015·2015-09-02

    Kroger Black Pepper Recalled Due to Salmonella Contamination

    Kroger is recalling Black Pepper Coarse Ground because a related product tested positive for Salmonella. The recall covers items produced on the same filling line.

    Product
    Kroger Black Pepper Coarse Ground UPC 11110 70041 NET WT 17.1 oz plastic container
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Drugs)·D-1357-2015·2015-09-02

    PharMEDium Recalls Heparin Sodium Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 240 bags of Heparin Sodium Injection USP 25,000 Units in 250 mL bags due to the presence of particulate matter.

    Product
    HEPARIN Sodium Injection USP 25,000 USP Units added to 250 mL 5% Dextrose Injection USP (100 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0419, NDC# 61553-419-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1356-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 48 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.

    Product
    EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Chloride Injection USP (64 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6618, NDC# 61553-618-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1358-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 264 bags of Epinephrine HCl injection due to the presence of particulate matter in the saline solution.

    Product
    EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Chloride Injection USP (16 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6119, NDC# 61553-119-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-3043-2015·2015-09-02

    Kroger Ground Cinnamon Recalled Due to Salmonella Risk on Filling Line

    The Kroger Co is recalling specific lots of Ground Cinnamon because a related product on the same line tested positive for Salmonella.

    Product
    Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-3046-2015·2015-09-02

    Kroger Artificial Bacon Flavored Chips Recalled Due to Salmonella Risk

    The Kroger Co is recalling specific lots of Kroger Bac'n Buds Artificial Bacon Flavored Chips because a related product tested positive for Salmonella.

    Product
    Kroger Bac'n Buds ARTIFICIAL BACON FLAVORED CHIPS 14.1oz plastic container UPC 0 11110 70025 4
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Drugs)·D-1354-2015·2015-09-02

    PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter

    PharMEDium Services is recalling 36 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.

    Product
    EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Chloride Injection USP (4 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6244, NDC# 61553-244-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·119-2015·2015-09-02

    Kenosha Beef Recalls Pork Sausage Patties Due to Metal Contamination

    Kenosha Beef International is recalling approximately 89,235 pounds of Johnsonville pork sausage patties that may contain small pieces of metal.

    Product
    Kenosha Beef International Ltd — Kenosha Beef Recalls Pork Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    11 states