The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

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.

6226–6250 of 7443

  • CriticalFDA (Food)·F-0217-2014·2013-11-27

    Terri Lynn Deluxe Mixed Nuts Recalled for Undeclared Peanuts

    Terri Lynn Inc. is recalling Deluxe Mixed Nuts labeled 'No Peanuts' because the bags contain undeclared peanuts.

    Product
    Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY; Terri Lynn Inc.; Deluxe Mixed; No Peanuts; NET WT. 16 OZ. (1 LB.) 454 g; P.O. BOX 5118 ELGIN, IL 60121
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0261-2014·2013-11-27

    Medtronic Cougar Nitinol Guidewires Recalled for Coating Delamination Risk

    Medtronic Vascular is recalling specific Cougar Nitinol Workhorse Guidewires because the PTFE coating may delaminate and detach from the device.

    Product
    Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ, CGRXT190HS, CGRXT190J, CGRXT190S, CGRXT300HJ, CGRXT300HS, CGRXT300J, CGRXT300S Medtronic guide wires are steerable guide wires that are used for the introduction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0183-2014·2013-11-27

    Trader Joe's Southwest Salad Recalled for Undeclared Soy

    World Class Distribution is recalling Trader Joe's Southwest Salad with Use by Date 11/2/13 due to undeclared soy.

    Product
    Trader Joe's Southwest Salads, 9oz. Packaged in plastic clamshell with ranch dressing packaged in plastic sealed solo cup. Product labeling reads in part:"TRADER JOE'S ***SOUTHWEST SALAD with Black Beans, Corn, Cotija Cheese and a tangy Ranch Dressing***NET WT. 9 OZ (255g)*
    Category
    Food
    Distribution
    5 states
  • CriticalCPSC·14028·2013-11-21

    Angelcare Baby Monitors Recalled for Infant Strangulation Hazard

    Angelcare is recalling about 600,000 baby monitors in the U.S. and 182,173 in Canada due to a strangulation risk from the sensor pad cord. Two infant deaths have been reported.

    Product
    Angelcare Movement and Sound Baby Monitors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1731-2013·2013-11-20

    Priester's Pecans Nutty Favorites Recalled for Salmonella Risk

    Priester Pecan Company is recalling Nutty Favorites Assortments because supplied pistachios may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand NUTTY FAVORITES ASST, Stock No. 79, Net Wt 1 lb 10 oz (737g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1732-2013·2013-11-20

    Priester's Pecans Roasted Nuts Recalled for Salmonella Risk

    Priester Pecan Company is recalling Fancy Roasted Nuts because pistachios supplied by ARO may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand FANCY ROASTED NUTS, Stock No. 7, Net Wt 12 oz (454g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0088-2014·2013-11-06

    Epicure Food Corp. Recalls St. Marcellin Cheese Due to Listeria Risk

    Epicure Food Corp. is recalling St. Marcellin cheese in several states because Listeria monocytogenes was detected in a related product in France.

    Product
    St. Marcellin Au lait pasteurise fabrique en Dauphine l'unite: poids net 80ge Fromagerie Qurtet 38470 VINAY
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-0085-2014·2013-11-06

    Conagra Recalls Pork & Leek Dumplings Due to Undeclared Allergens

    Conagra is recalling specific lots of P.F. Chang's Pork & Leek Dumplings because they were inadvertently packaged with Shrimp & Pollack Fish dumplings, resulting in undeclared allergens.

    Product
    P.F. Chang's Home Menu, Pork & Leek Dumplings, frozen, packaged in 12.5 oz bags. UPC: 0 36200 21215 8
    Category
    Food
    Distribution
    33 states
  • CriticalFDA (Food)·F-0086-2014·2013-11-06

    Schwebel's Golden Rich Buns Recalled for Undeclared Eggs

    Schwebel Baking Company is recalling Golden Rich Buns with Honey because they contain undeclared eggs. The product was distributed to six states.

    Product
    Schwebel's Golden Rich Bun with Honey, 18 oz plastic bag, 12 count, UPC 0 71319 00083 8 Product labeled in part, "INGREDIENTS: ENRICHED WHEAT FLOUR***CONTAINS: WHEAT, SOY SCHWEBEL BAKING CO. YOUNGSTOWN, OH 44501"
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-2298-2013·2013-10-09

    MedStream Refill Kit Recalled for Excessive Drug Flow Rates

    Codman & Shurtleff, Inc. is recalling MedStream Refill Kits because they may deliver drug flow rates exceeding programmed levels.

    Product
    MedStream Refill Kit, U.S (6 units): 91-4288 Product Usage: The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2295-2013·2013-10-09

    MedStream Refill Kit Recalled for Excessive Drug Flow Rates

    Codman & Shurtleff is recalling MedStream Refill Kits because they may deliver drug flow rates exceeding programmed levels.

    Product
    MedStream Refill Kit, U.S: 91-4287 Product Usage: The Medstream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market. Refill Kits- are intended for use in the fillin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1910-2013·2013-10-02

    Bubbles Baking Blueberry Muffins Recalled for Undeclared Milk and Soy

    Bubbles Baking Co. is recalling First Street Blueberry Muffins Loaf because they may contain undeclared milk and soy allergens.

    Product
    First Street Blueberry Muffins Loaf (S 45383), 16 oz., 12 trays/case, UPC 0 41512 10854 9.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1902-2013·2013-09-25

    JTM Provisions Recalls Bean and Cheese Burrito Filling for Undeclared Eggs

    JTM Provisions Co Inc is recalling 10 lb bags of Bean & Cheese Burrito Filling because the product contains undeclared eggs.

    Product
    Bean & Cheese Burrito Filling, 10 lb bags Labeled in part "13210 B 1 77220 13:38 KEEP FROZEN BEAN & CHEESE BURRITO FILLING***INGREDIENTS: COOKED PINTO BEANS, WATER, CHEDDAR CHEESE***SOYBEAN OIL***STARCH-MODIFIED, ONIONS, CHEESE SAUCE BASE***CONTAINS LESS THAN 2% OF CHILI PEPPER,
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2125-2013·2013-09-18

    Siemens Microscan plus Negative Urine Combo 4 Recalled for Misreads

    Siemens Healthcare Diagnostics is recalling Microscan plus Negative Urine Combo 4 panels due to confirmed false susceptible and intermediate misreads for specific antibiotics.

    Product
    Microscan plus Negative Urine Combo 4 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2126-2013·2013-09-18

    Siemens Microscan Plus Negative Breakpoint Combo 4 Recalled for Misreads

    Siemens Healthcare Diagnostics is recalling Microscan plus Negative Breakpoint Combo 4 panels due to confirmed false susceptible and intermediate misreads for specific antibiotics.

    Product
    Microscan plus Negative Breakpoint Combo 4 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification fo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2123-2013·2013-09-18

    Siemens Microscan Synergies Plus Negative Urine Combo 5 Recall

    Siemens is recalling Microscan Synergies Plus Negative Urine Combo 5 panels due to confirmed false susceptibility results for imipenem and meropenum.

    Product
    Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-negative bacte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2124-2013·2013-09-18

    Siemens Microscan Plus Negative Combo 3 Recalled for Misreads

    Siemens Healthcare Diagnostics is recalling Microscan plus Negative Combo 3 panels due to confirmed false susceptible and intermediate misreads for imipenem and meropenum.

    Product
    Microscan plus Negative Combo 3 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-nega
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1866-2013·2013-09-11

    Kroger Cookie Dough Recalled for Undeclared Peanut Allergen

    Conagra is recalling Kroger Break 'N Bake Chocolate Chip Cookie Dough because peanut butter was present but not listed on the label.

    Product
    Kroger Break 'N Bake Chocolate Chip Cookie Dough, refrigerated dough, packaged in 16.0 oz. plastic package.
    Category
    Food
    Distribution
    26 states
  • CriticalFDA (Drugs)·D-929-2013·2013-09-11

    FDA Recalls SexVoltz Herbal Supplement Containing Unapproved Tadalafil

    Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.

    Product
    SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 and 12 capsule bottles, Manufactured For: BeaMonstar Products, Queen Creek, AZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-930-2013·2013-09-11

    Velextra Herbal Supplement Recalled for Containing Unapproved Tadalafil

    Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.

    Product
    Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1865-2013·2013-09-11

    Zip International Recalls Baltic Sprats in Spicy Brine Due to Listeria Risk

    Zip International Group LLC is recalling Baltic Sprats in Spicy Brine because the product may be contaminated with Listeria monocytogenes.

    Product
    Baltic Sprats in Spicy Brine Net Wt. 15.8 oz. Prod. of Latvia Distributed by Zip International Group LLC 160 Raritan Center Parkway Unit #6 Edison NJ 08837 T 732-225-3600 UPC 4750217602547
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-922-2013·2013-09-04

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.

    Product
    0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1854-2013·2013-09-04

    Heeren Brothers Recalls Athena Cantaloupes Due to Listeria Contamination

    Heeren Brothers Produce is recalling Athena cantaloupes sold in Michigan after FDA testing found Listeria monocytogenes contamination.

    Product
    Cardboard BIN LABEL: 03808 LOT #: 09000101, MELON CANTALOUPE..., 80-90 CT , 07/22/13 cantaloupes themselves are not labeled.
    Category
    Food
    Distribution
    1 state