The Recall Desk

Severity 1 of 5

Low recalls

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

What “low” means here

Severity 1 (Low) recalls are typically cosmetic defects, documentation issues, packaging-only problems, and Class III administrative corrections. The product itself is unlikely to cause adverse health consequences. The manufacturer is correcting the issue to comply with FDA or USDA rules, not because anyone is at risk. You can almost always continue using a Severity-1 product without concern.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

1676–1700 of 2769

  • LowFDA (Food)·F-1269-2016·2016-05-04

    Bliss Bros Dairy Recalls Cresent Ridge Choc Chip Cookie Dough

    Bliss Bros Dairy is recalling 5 units of Cresent Ridge Choc Chip Cookie Dough because the product failed to meet air space specifications.

    Product
    Cresent Ridge Choc Chip Cookie Dough 48oz Product Code: 35418
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1277-2016·2016-05-04

    Bliss Bros Dairy Recalls Emack & Bolios Ice Cream for Air Space Issues

    Bliss Bros Dairy is recalling 50 units of Emack & Bolios Stoney's Dream Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Stoney's Dream Ice Cream, 3gal Product Code: 36276
    Category
    Food
    Distribution
    7 states
  • LowFDA (Devices)·Z-1582-2016·2016-05-04

    Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label

    Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.

    Product
    Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1276-2016·2016-05-04

    Bliss Bros Dairy Recalls Emack & Bolios Grasshopper Ice Cream

    Bliss Bros Dairy is recalling 240 units of Emack & Bolios Grasshopper Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Grasshopper Ice Cream 3gal Product Code: 36272
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1279-2016·2016-05-04

    Bliss Bros Dairy Recalls Pistachio Ice Cream for Packaging Defect

    Bliss Bros Dairy is recalling Emack & Bolios Pistachio Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Pistachio Ice Cream, 3gal Product Code: 36262
    Category
    Food
    Distribution
    7 states
  • LowFDA (Drugs)·D-0834-2016·2016-05-04

    SKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling

    McKesson Packaging Services is recalling SKY Aspirin Chewable Tablets because the outer cartons were incorrectly labeled. The recall addresses a labeling mix-up.

    Product
    SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Service, Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1253-2016·2016-05-04

    Suan's Scotch Bonnet Pepper Relish Recalled for Swollen or Leaking Lids

    S & S Foods, Inc. is recalling 262 jars of Suan's Scotch Bonnet Pepper Relish in Oklahoma due to reports of swollen or leaking lids.

    Product
    Suan's Scotch Bonnet Pepper Relish 9.8 oz. packaged in a glass jar with a metal lid.
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1275-2016·2016-05-04

    Emack & Bolios Ice Cream Recalled for Air Space Specification Failures

    Bliss Bros Dairy is recalling Emack & Bolios Caramel Moose Prints Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Caramel Moose Prints Ice Cream, 3gal Product Code: 36285
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1281-2016·2016-05-04

    Bliss Bros Dairy Recalls Emack & Bolios Space Cake Ice Cream

    Bliss Bros Dairy is recalling Emack & Bolios Space Cake Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Space Cake Ice Cream, 3gal Product Code: 36273
    Category
    Food
    Distribution
    7 states
  • LowFDA (Devices)·Z-1509-2016·2016-04-27

    OraSure Recalls OraQuick HCV Visual Reference Panel Due to Incorrect Insert

    OraSure Technologies is recalling 244 OraQuick HCV Visual Reference Panel kits because the package insert may be incorrect, potentially containing instructions for a different test.

    Product
    OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with antibody levels near the limit of detection of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0824-2016·2016-04-27

    Telmisartan Tablets Recalled Due to Presence of Silicone Foreign Matter

    Torrent Pharmaceuticals is recalling Telmisartan 80 mg tablets because a product complaint identified silicone foreign matter within the tablets.

    Product
    Telmisartan Tablets, USP, 80 mg, 30-count (3 x 10 unit-dose blisters) per carton, Rx only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, Dist. Mehsana, INDIA.; For: Torrent Pharma Inc., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920, NDC 13668-158-72, UPC 3 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·16V237000·2016-04-22

    Forest River Recalls Prime Time Crusader Trailers for Incorrect Federal Placard

    Forest River is recalling 2015-2017 Prime Time Crusader trailers because the Federal Placard incorrectly lists the Cargo Carrying Capacity. Dealers will install corrected placards free of charge.

    Product
    PRIME TIME — PRIME TIME CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0869-2016·2016-04-20

    Morrison's Cornbread Mix Recalled for Potential Metal Fragments

    Morrison's Home Style Cornbread Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Morrison's Home Style Cornbread Mix NET WT 5 LB (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1350-2016·2016-04-20

    Siemens Recalls One CT System Due to Front Cover Welding Defect

    Siemens is recalling one SOMATOM Definition AS CT system because a front cover weld defect could cause a bolt to break during service, though no clinical risk exists.

    Product
    SOMATOM Definition AS, a family of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission dta from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0818-2016·2016-04-20

    Fresenius Kabi Recalls Haloperidol Decanoate Injection Due to Impurity

    Fresenius Kabi USA, LLC is recalling Haloperidol Decanoate Injection due to an impurity out-of-specification result. The recall affects 48,210 units distributed nationwide and in Puerto Rico.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0872-2016·2016-04-20

    Ben E. Keith Cornbread Mix Recalled for Metal Fragments

    Morrison Milling is recalling Ben E. Keith Home Style Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Ben E. Keith Home Style Cornbread Mix NET WT 5 lb. (2.27kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0834-2016·2016-04-20

    Morrison Milling Recalls HEB Cheddar Bacon Cornbread Mix for Metal Fragments

    Morrison Milling is recalling HEB Cheddar Bacon Flavored Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    HEB Cheddar Bacon Flavored Cornbread Mix NET WT. 13.3 OZ (377g) packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0822-2016·2016-04-20

    Amerisource Health Services Recalls Fenofibrate Capsules Due to Labeling Errors

    Amerisource Health Services is recalling 228 cartons of Fenofibrate Capsules because some units have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217, Carton of 20: NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0895-2016·2016-04-20

    Razzoo's Seasoned Corn Flour Recalled for Potential Metal Fragments

    Morrison Milling is recalling Razzoo's Seasoned Corn Flour because it may contain small metal fragments from a wire mesh sifter.

    Product
    Razzoo's Seasoned Corn Flour NET WT 25 LB (11.33 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0820-2016·2016-04-20

    Impax Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Impax Laboratories is recalling 28,001 bottles of Fenofibrate Capsules (Micronized) 134 mg because the bottles have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
    Category
    Drug
    Distribution
    Distributed nationwide