The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

35851–35875 of 50504

  • HighFDA (Food)·F-1302-2016·2016-05-11

    North Fish USA Recalls Cold Smoked Saury Due to Sanitary Violations

    North Fish USA is recalling cold smoked saury because the Florida Department of Agriculture found the products were not produced under an adequate HACCP plan and held in unsanitary conditions.

    Product
    Cold smoked Saira (Saury), vacuum packaged, 3 pieces per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1303-2016·2016-05-11

    North Fish USA Recalls Cold Smoked Mackerel Due to Sanitation Issues

    North Fish USA is recalling cold smoked mackerel because it was not produced under an adequate HACCP plan and was held in unsanitary conditions.

    Product
    Cold smoked Mackerel, vacuum packaged, one fish per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·16V286000·2016-05-11

    Great Lakes Drywall Pup Trailers Recalled for Rear Impact Guard Defect

    Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.

    Product
    GREAT LAKES — GREAT LAKES DRYWALL PUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1300-2016·2016-05-11

    North Fish USA Recalls Hot Smoked Mackerel Due to Sanitary Issues

    North Fish USA is recalling hot smoked mackerel because the Florida Department of Agriculture found it was not produced under an adequate HACCP plan and was held in unsanitary conditions.

    Product
    Hot smoked Mackerel, vacuum packaged, one fish per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1307-2016·2016-05-11

    R.W. Bakers Recalls Dinner Rolls for Undeclared Peanuts

    R.W. Bakers Co. is recalling specific packages of dinner rolls and plain knot rolls because they may contain undeclared peanuts.

    Product
    Assorted Dinner Rolls, 128 ct., Net Wt. 10.2 lbs; 16/ 8 ct./case
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1598-2016·2016-05-11

    Siemens MAGNETOM MRI Systems Recalled Due to Magnetic Table Cover Hazard

    Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.

    Product
    MAGNETOM Aera/Skyra Systems, whole body magnetic resonance imaging systems, Model numbers 10432914, 10432915. Docking station top cover (part no# 10591430) of the removable patient table.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1310-2016·2016-05-11

    Specialty Produce Recalls Diced Red Potatoes for Undeclared Sulfites

    Specialty Produce Corporation is recalling diced red potatoes in Rhode Island due to undeclared sulfites. The recall was initiated voluntarily by the firm.

    Product
    Diced Red Potatoes, hand labeled: "Potato, Red Dice, 40# 3/4 large"
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1611-2016·2016-05-11

    Applied Medical Recalls Wilson Implantation System Due to Sterilization Breach

    Applied Medical Technology Inc is recalling 1,100 units of the Wilson Implantation System after a complaint revealed an open pouch that breached sterilization validation.

    Product
    Wilson Implantation System Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-1609-2016·2016-05-11

    Applied Medical Technology Recalls Self-Retaining Retractor Frames Due to Sterilization Breach

    Applied Medical Technology is recalling 3,754 units of TLC Self-Retaining Retractor Frames because a complaint reported an open pouch, which breaches sterilization validation.

    Product
    TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) STERILE EO Do Not Resterilize. Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Food)·F-1305-2016·2016-05-11

    North Fish USA Recalls Hot Smoked Escolar Chunks Due to Sanitation Issues

    North Fish USA is recalling 40 packages of hot smoked Escolar chunks because they were not produced under an adequate HACCP plan and were held in unsanitary conditions.

    Product
    Hot smoked Escolar chunks, vacuum packaged, one chunk per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1299-2016·2016-05-11

    North Fish USA Recalls Hot Smoked Atlantic Ocean Perch for Sanitation Issues

    North Fish USA is recalling hot smoked Atlantic Ocean Perch because the Florida Department of Agriculture found the products were not produced under an adequate HACCP plan and were held in unsanitary conditions.

    Product
    Hot smoked Atlantic Ocean Perch, vacuumed package, one fish per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1294-2016·2016-05-11

    DMH Ingredients Recalls Organic Lemon Myrtle Due to Salmonella

    DMH Ingredients Inc is recalling 20 cases of Organic Lemon Myrtle because the product tested positive for Salmonella. The product was distributed to one manufacturer in New Jersey.

    Product
    Organic Lemon Myrtle packed in a 12.5kg plastic bag inside of a cardboard box.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1312-2016·2016-05-11

    QTrade Recalls Organic Chamomile Tea Due to Salmonella Risk

    QTrade Teas & Herbs is recalling Organic Chamomile Tea Bag Cut because it may be contaminated with Salmonella. The product was distributed in New Jersey and Ohio.

    Product
    Organic Chamomile Tea Bag Cut (TBC) bulk sold in original cases (25kg bags), Bulk product 25 kg craft paper bags "L 0609-13681-238641-01 ORGANIC CHAMOMILE TBC CERTIFIED ORGANIC MATRICARIA CHAMOMILLA 25KG NET ORIGIN: COSOVO WORLEE HAMBURG"
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1313-2016·2016-05-11

    Sincere Orient Thin Egg Noodles Recalled for Undeclared Wheat

    Sincere Orient Commercial Foods Corp. is recalling Thin Egg Noodles (Mi Trung Ga) because they contain undeclared wheat.

    Product
    Thin Egg Noodle (Mi Trung Ga), 5lbs, 8 units/case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1608-2016·2016-05-11

    Applied Medical Recalls TLC Self Retaining Retractor Systems Due to Sterilization Breach

    Applied Medical Technology Inc is recalling 5,334 units of TLC Self Retaining Retractor Systems because a complaint reported an open pouch that breaches sterilization validation.

    Product
    TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Food)·F-1297-2016·2016-05-11

    North Fish USA Recalls Salted Herring Due to Sanitary Violations

    North Fish USA is recalling salted herring because it was not produced under an adequate HACCP plan and was held in unsanitary conditions.

    Product
    Salted Herring in pail, 30 pieces per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1101-2016·2016-05-11

    Pastry Food Products Recalls TRIGAL Empanadillas for Undeclared Allergens

    Pastry Food Products Inc. is recalling TRIGAL Empanadillas Sabor a Carne due to undeclared yellow #5 and soy protein. The product was distributed in Puerto Rico.

    Product
    TRIGAL*** Empanadillas Sabor a Carne (meat flavored turnovers)***Peso neto 3 lbs (Net Weight 3 pounds)*** Pqte. de 12 (12 units package)***Pastry Foods Inc. Rio Piedras PR
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1295-2016·2016-05-11

    North Fish USA Recalls Cold Smoked White Fish Due to Sanitation Issues

    North Fish USA is recalling cold smoked white fish because it was not produced under an adequate HACCP plan and was held in unsanitary conditions.

    Product
    Cold smoked white fish, vacuum packaged, one fish per package. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1600-2016·2016-05-11

    Nuvectra Algovita Spinal Cord Stimulation Programmer Recall for Software Defect

    Nuvectra is recalling 17 Algovita Spinal Cord Stimulation System Clinical Programmers (Model 4500) because a software defect may prevent users from recharging the implantable pulse generator.

    Product
    Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use with Algovita Spinal Cord Stimulation Systems. The version of the software in the Clinician Programmer is v1.1.5. The Algovita Spinal Cord Stimulation system consists of a stimulator…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1311-2016·2016-05-11

    Wise Foods Recalls Potato Chips With Undeclared Wheat Allergen

    Wise Foods is recalling 400 bags of Cha-Ching Original Potato Chips because the packaging was filled with BBQ Seasoned product containing undeclared wheat.

    Product
    Cha-Ching Original Potato Chips Net Wt 10 OZ.; Distributed by OZA Brands, LLC, Salisbury, NC 28147
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1301-2016·2016-05-11

    North Fish USA Recalls Sliced Cold Smoked Escolar Due to Sanitation Issues

    North Fish USA is recalling sliced cold smoked Escolar because it was not produced under an adequate HACCP plan and was held in unsanitary conditions.

    Product
    Sliced cold smoked Escolar, 8 oz and 1 lb, vacuum packaged. Manufactured by North Fish USA, Pembroke Pines, FL 33009
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1306-2016·2016-05-11

    Meijer Plain Knot Rolls Recalled for Undeclared Peanuts

    R.W. Bakers Co. is recalling Meijer Plain Knot Rolls and Assorted Dinner Rolls due to potential undeclared peanuts.

    Product
    Meijer Plain Knot Rolls, 8 ct., Net Wt. 10 oz.; 12/case, 9.4 lbs/case
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1103-2016·2016-05-11

    Trigal Coconut Arepas Recalled for Undeclared Sodium Metabisulfite Allergen

    Pastry Food Products Inc. is recalling Trigal Coconut Flavored Arepas due to undeclared sodium metabisulfite. The product was distributed in Puerto Rico.

    Product
    Trigal***Arepas de Coco (Coconut Flavored Arepas)***Mant¿ngase refrigerado (Keep refrigerated)***Peso Neto 1.12 lb (509 g)***Paquete de 12 (12 units package)***Manufacturado Por (Manufactured by): Pastry Foods Inc.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1586-2016·2016-05-11

    Ab Sciex Analyst MD Software Recall for Incorrect Diagnostic Results

    Ab Sciex is recalling Analyst MD software versions 1.6.1 and 1.6.2 because it may display wrong quantitative results, potentially leading to incorrect patient diagnoses.

    Product
    Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP¿ LC/MS/MS System, Instrument Part Number: 5024500; Triple Quad" 4500MD LC/MS/MS System, Instrument Part Number: 5031257…
    Category
    Medical Device
    Distribution
    Distributed nationwide