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.

Filters

Agency

Category

Minimum severity

Clear filters

22651–22675 of 39699

  • SevereFDA (Devices)·Z-0044-2017·2016-10-26

    Teleflex Medical Recalls Willy Rusch Tracheostomy Tube Sets

    Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.

    Product
    Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0205-2017·2016-10-26

    QualiTech Recalls FE Rainbow Blend Due to Potential E. coli O121 Presence

    QualiTech, Inc. is recalling 1,400 lbs of FE Rainbow Blend because a supplier notified the company of potential E. coli O121 bacteria in the material.

    Product
    FE Rainbow Blend, Product Code 22795. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0180-2017·2016-10-26

    Windstone Medical Packaging Recalls Endoscopy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.

    Product
    Endoscopy Pack, Kit number PSS1646 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0107-2017·2016-10-26

    Dream Body Weight Loss Capsules Recalled for Undeclared Sibutramine

    Dream Body Weight Loss is recalling Dream Body 450 mg capsules because they contain undeclared sibutramine and were marketed without FDA approval.

    Product
    Dream Body 450 mg 30 capsules in a plastic screw on top bottle
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0290-2017·2016-10-26

    RTI Surgical Recalls Streamline OCT Spinal Rods Due to Cracks

    RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.

    Product
    RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3), the Streamline OCT Occipito-Cervico-Thoracic System is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0193-2017·2016-10-26

    QualiTech Recalls FE Bacon 286 Due to Potential E. coli O121 Presence

    QualiTech is recalling 400 lbs of FE Bacon 286 because a supplier reported the potential presence of E. coli O121 bacteria.

    Product
    FE Bacon 286, Product Code 22286. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0224-2017·2016-10-26

    Fresh From Texas Recalls HEB Ready Fresh Go Carrots and Apples

    Fresh From Texas Inc. is recalling HEB Ready Fresh Go Carrots and Apples due to potential Listeria monocytogenes contamination.

    Product
    HEB Ready Fresh Go Carrots, Apples with Yogurt Pretzels and Ranch Dip 4.75 oz. UPC 4122002119 packaged in clear plastic tray
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0118-2017·2016-10-26

    Awareness Boost Tea Recalled for Potential Salmonella Contamination

    Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.

    Product
    Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness Corporation P.O. Box 2289 Chandler, AZ 85244
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0216-2017·2016-10-26

    Fresh From Texas Recalls Apples for Listeria Contamination Risk

    Fresh From Texas Inc. is recalling 34,425 units of packaged apples in Texas due to potential Listeria monocytogenes contamination.

    Product
    Red & Green Apples Large 17 oz. UPC 4122087649 packaged in clear plastic container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0223-2017·2016-10-26

    Fresh From Texas Recalls HEB Ready Fresh Go Carrots and Apples

    Fresh From Texas Inc. is recalling HEB Ready Fresh Go Carrots, Apples with Sesame Sticks & Hummus due to potential Listeria monocytogenes contamination.

    Product
    HEB Ready Fresh Go Carrots, Apples with Sesame Sticks & Hummus 6 oz. UPC 4122002144 packaged in clear plastic tray
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0185-2017·2016-10-26

    Windstone Medical Packaging Recalls Extremity Tray Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Extremity Tray, Kit number AMS1200(B and AMS1200(C convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0127-2017·2016-10-26

    X Spine Systems Recalls Calix T PEEK Lumbar System Trial Devices

    X Spine Systems is recalling 1,186 Calix T PEEK Lumbar System trial devices because components may detach and lodge in the intervertebral space during surgery.

    Product
    Calix T PEEK Lumbar System, TLIF Trial
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-0199-2017·2016-10-26

    QualiTech Red Bell Pepper Recalled for Potential E. coli O121 Contamination

    QualiTech is recalling 4,150 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed in ten US states and Canada.

    Product
    FE Red Bell Pepper, Product Code 22708. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0195-2017·2016-10-26

    QualiTech Recalls Green Bell Peppers Due to Potential E. coli O121 Contamination

    QualiTech, Inc. is recalling 300 lbs of green bell peppers due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.

    Product
    FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0233-2017·2016-10-26

    Windstone Medical Packaging Recalls Major Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Major Laparotomy Pack - NS, kit number AMS4347 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0108-2017·2016-10-26

    Dream Body Advanced capsules recalled for undeclared sibutramine

    Dream Body Advanced 400 mg capsules are being recalled because they contain undeclared sibutramine and were marketed without an approved NDA/ANDA.

    Product
    Dream Body Advanced 400 mg 30 capsules in brown foil packets.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0126-2017·2016-10-26

    X Spine Systems Recalls Calix T PEEK Lumbar System TLIF Rasps

    X Spine Systems is recalling 195 units of Calix T PEEK Lumbar System TLIF Rasps because the tools may detach and become lodged in the surgical site.

    Product
    Calix T PEEK Lumbar System, TLIF Rasp
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-0203-2017·2016-10-26

    QualiTech Recalls Frozen Red Bell Peppers Due to E. coli O121 Risk

    QualiTech is recalling frozen red bell peppers due to a potential presence of E. coli O121 bacteria reported by a supplier.

    Product
    FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0225-2017·2016-10-26

    Fresh From Texas Recalls HEB Fruit Cups for Listeria Risk

    Fresh From Texas Inc. is recalling HEB Ready Fresh Go fruit cups due to potential Listeria monocytogenes contamination. The product was distributed in Texas.

    Product
    HEB Ready Fresh Go Pineappple, Grapes & Apples with Banana Chips 6 oz. UPC 4122002138 packaged in clear plastic tray
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0198-2017·2016-10-26

    QualiTech Recalls Cheddar Cheese Due to Potential E. coli O121 Presence

    QualiTech is recalling FE Cheddar Cheese because a supplier reported the potential presence of E. coli O121 bacteria.

    Product
    FE Cheddar Cheese, Product Code 22518. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0146-2017·2016-10-26

    Fresh Express American Salad Recalled for Incorrect Condiment Kits

    Fresh Express is recalling American Salad bags that may contain incorrect condiment kits. Consumers in six states should check their products.

    Product
    Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0263-2017·2016-10-26

    Windstone Medical Recalls Plastic Packs with Defective Gloves

    Windstone Medical Packaging is recalling 204 plastic packs used in general surgery because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Plastic Pack , Kit number AMS1833(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0219-2017·2016-10-26

    Fresh From Texas Recalls Apples and Grapes Due to Listeria Risk

    Fresh From Texas Inc. is recalling 10-ounce packages of Apples & Grapes sold in Texas due to potential Listeria monocytogenes contamination.

    Product
    Apples & Grapes 10 oz. UPC 4122087666 packaged in clear plastic container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0162-2017·2016-10-26

    Union Bagel Shop Cowboy Cookies Recalled for Undeclared Allergens

    Union Bagel Shop is recalling Cowboy Cookies In-a-Jar because the packaging fails to declare wheat, milk, and soy allergens.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Cowboy Cookies In-a- Jar***INGREDIENTS: FLOUR, ROLLED OATS, BROWN SUGAR, BAKING POWDER, SALT, SUGAR, M & M's***" This information was hand written on a business card, no separate ingredient statement.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0202-2017·2016-10-26

    QualiTech Recalls Green Bell Peppers Due to E. coli O121 Risk

    QualiTech, Inc. is recalling specific lots of green bell peppers due to a potential presence of E. coli O121 bacteria identified by a supplier.

    Product
    FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states