The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

28526–28550 of 32252

  • SevereNHTSA·13E017000·2013-04-11

    Takata Frontal Passenger Air Bag Inflator Recall for Rupture Risk

    Takata is recalling certain frontal passenger-side air bag inflators that may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V137000·2013-04-11

    KME Emergency Vehicles Recalled for Potential Brake Fire Risk

    Kovatch is recalling specific KME emergency vehicles because brake chambers may leak, causing the parking brake to drag and potentially leading to overheated components and fire.

    Product
    KME — KME PANTHER, PREDATOR SS, PANTHER II, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-239-2013·2013-04-10

    Dr. Reddy's Recalls Amoxicillin Oral Suspension Due to Microbial Contamination

    Dr. Reddy's is recalling specific lots of Amoxicillin for Oral Suspension because testing revealed yeast and mold growth.

    Product
    Amoxicillin for Oral Suspension, 125mg/5mL, a) 80 mL (NDC 43598-222-80); b) 100mL, (NDC 43598-222-52); c)150 mL (NDC 43598-222-53) bottles, Rx only, Dist. By: Dr. REDDY'S Laboratories, Inc., Bridgewater, NJ 08807
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-231-2013·2013-04-10

    FDA Recalls Unapproved Nootropa Cognitive Enhancement Supplement

    Palmer Natural Products is recalling Nootropa Cognitive Enhancement Supplement because it was marketed without an approved NDA/ANDA.

    Product
    NOOTROPA COGNITIVE ENHANCEMENT SUPPLEMENT, 400 mg Aniracetam Capsules 60 count bottle, OTC Manufactured & Packaged in the USA for NOOTROPA.COM. DEVELOPED BY: Digital Superfuture Limited Arntel Building 9B 148 Des Voeux Rd. Hong Kong.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Food)·F-1285-2013·2013-04-10

    Sweet P's Bake Shop Caramel Apple Danish Coffee Cake Recalled for Undeclared Walnuts

    Gold Standard Baking, Inc. is recalling Sweet P's Bake Shop Caramel Apple Danish Coffee Cakes because they contain undeclared walnuts. The affected products were distributed in Illinois.

    Product
    Sweet P's Bake Shop branded Caramel Apple Danish Coffee Cake, 14 oz, in a plastic clamshell package, UPC Code: 011225113833
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1286-2013·2013-04-10

    Beehive Botanicals Recalls Propolis Powder Due to Fluvalinate Contamination

    Beehive Botanicals, Inc. is recalling specific lots of Propolis Powder because they tested positive for Fluvalinate.

    Product
    Propolis Powder -100% Standardized Bee-Propolis Lot #: 021113-55/60, EXP: 10/14 11# Bag & Lot#: 10081155/60-120612-100, EXP: 12/15, 1# BAG.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1279-2013·2013-04-10

    Green Day Dried Coconut Recalled for Undeclared Sulfites

    Domega NY International Co. is recalling Green Day Dried Coconut due to undeclared sulfites detected by New York State testing.

    Product
    GREEN DAY DRIED COCONUT, Net Wt: 3oz (85g), UPC bar code 6 950296 800744 -- Manufacturer: Jiangmen Xinhui Parksun Food Co., Ltd. -- Add: Donggua Hill, Beitou Village, Qibao, Xinhui District, Jiangmen City, Guangdong, Produce of P.R.C. -- Packed For: Domega NY International Co.…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1294-2013·2013-04-10

    Producers Peanut Company Recalls Peanut Granules Due to Aflatoxin Concerns

    Producers Peanut Company is recalling America Farm Peanut Granules because they may contain aflatoxins above allowable levels. The product was distributed in five US states and Barbados.

    Product
    America Farm Peanut Granules, bulk packed in 30 lb plastic bags in a box, and labeled in part ***Manufactured by Producers Peanut Co., Inc. 337 Moore Ave., Suffolk, VA 23434***
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1045-2013·2013-04-10

    Zimmer NexPosure Retractor Portals Recalled for Sterility Risk

    Zimmer, Inc. is recalling 58 NexPosure retractor portals due to a potential breach in the sterile inner pouch, which could lead to product contamination and patient infection.

    Product
    Zimmer NexPosure, retractor portals of the NexPosure MIS Access System, Part Numbers or REF numbers: N1830R80-100, N1830R80-090¿, N1830R80-080¿, N1830R80-070¿, N1830R80-060, N1830R50-100, N1830R50-090, N1830R50-080, ¿ N1830R50-070, N1830R50-060, N1830L80-100, N1830L80-090…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0993-2013·2013-04-10

    Animas 2020 Insulin Pump Recall for False Alarm Component Issue

    Animas Corporation is recalling 7,157 Animas 2020 insulin pumps due to a component issue that may cause false alarms for loss of prime, occlusion, or no cartridge detected.

    Product
    Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-242-2013·2013-04-10

    West-Ward Recalls Subpotent Ethambutol Hydrochloride Tablets

    West-Ward Pharmaceutical Corp. is recalling 3,061 bottles of Ethambutol Hydrochloride Tablets due to out-of-specification assay results.

    Product
    Ethambutol Hydrochloride Tablets, USP, 100 mg, 100-count tablets per bottle, Rx only, Mfd. for: Versapharm Incorporated, Marietta, GA; Mfd. by: West-Ward Pharmaceutical Corp., Eatontown, NJ 07724; NDC 61748-011-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-233-2013·2013-04-10

    Unapproved Piracetam and Choline Capsules Recalled by FDA

    Palmer Natural Products is recalling unapproved Piracetam and Choline capsules marketed without FDA approval.

    Product
    Piracetam & Choline, 390mg Piracetam 104mg Choline Capsules, a) 30 count bottle, b) 100 count bottle, OTC, BoostYourGrade, LLC, Orlando, FL. 32826 ,
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1014-2013·2013-04-10

    Smiths Medical Recalls BCI Remote Alarm Cables for Capnograph Systems

    Smiths Medical is recalling 39 BCI Remote Alarm Cables because they may fail to transfer alarm signals to remote nurse alarm systems.

    Product
    Smiths Medical, BCI¿ Remote Alarm Cable (Normally Open & Normally Closed), Reorder Numbers: WW3398NO & WW3398NC. For use with respiration carbon dioxide measurement equipment. Product Usage: The BCI¿ Remote Alarm Cable is designed for use with the 9004 Capnocheck¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-243-2013·2013-04-10

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira is recalling 624,240 units of 0.9% Sodium Chloride Injection, USP, 50 mL, due to a lack of assurance of sterility and potential leakage.

    Product
    0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36 Hospira, Inc., Lake Forest, IL 60045
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1293-2013·2013-04-10

    Producers Peanut Company Recalls Peanut Butter for Aflatoxin Contamination

    Producers Peanut Company is recalling bulk peanut butter products because they may contain aflatoxins above allowable levels.

    Product
    Bulk Creamy/Smooth Peanut butter, packed in plastic 4 lb tub, packed 6 tubs/box; 5 lb tub, packed 6 tubs/box, and 35 lb buckets under private labels: Peanut Kids, Eden and American Farm Peanut Butters, and labeled in part ***Manufactured by Producers Peanut Co., Inc. 337 Moore…
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·13V131000·2013-04-10

    NABI Transit Buses Recalled for Defroster Switch Fire Risk

    North American Bus Industries is recalling 2008-2013 NABI 416 and 2012 31LFW buses because the defroster switch may overheat, melt the dash, or cause a fire.

    Product
    NABI — NABI 416, 31LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1292-2013·2013-04-10

    Producers Peanut Company Recalls Happy Kids Crunchy Peanut Butter for Aflatoxin Risk

    Producers Peanut Company is recalling Happy Kids Crunchy Peanut Butter because it may contain aflatoxins above allowable levels. The product was distributed in several US states and Barbados.

    Product
    Happy Kids Crunchy Peanut butter, packed in 8 oz, 12 oz, 28 oz, packed 12 jars/cs and 40 oz jars, packed 6 jars/cs; jars are labeled in part ***Manufactured by Producers Peanut Co., Inc. 337 Moore Ave., Suffolk, VA 23434***
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1291-2013·2013-04-10

    Producers Peanut Company Recalls Happy Kids Creamy Peanut Butter

    Producers Peanut Company is recalling Happy Kids Creamy Peanut Butter because it may contain aflatoxins above allowable levels.

    Product
    Happy Kids Creamy Peanut Butter, packed in 8 oz, 12 oz, 28 oz, 40 oz jars; packed 12 jars/box and 6 jars/box (40 oz), and labeled in part ******Manufactured by Producers Peanut Co., Inc. 337 Moore Ave., Suffolk, VA 23434***
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·13V135000·2013-04-10

    Temsa TS30 and TS35C Motor Coach Buses Recalled for Brake Gauge Defects

    Temsa is recalling 2011-2013 TS35C and 2012-2013 TS30 motor coach buses because air brake gauges and ABS indicators may fail to display accurate information, increasing crash risk.

    Product
    TEMSA — TEMSA TS30, TS35C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V129000·2013-04-09

    Load Trail Recalls 2011-2012 Load Max HD Goosenecks for Brake Failure

    Load Trail is recalling 2011-2012 Load Max HD Goosenecks because hydraulic brake actuators may fail, causing loss of braking ability and increasing crash risk.

    Product
    LOAD MAX — LOAD MAX HD GOOSENECKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V125000·2013-04-09

    Blue Bird Recalls 2008-2011 All American School Buses for Fire Risk

    Blue Bird is recalling 2008-2011 All American school buses because an improperly routed power cable could chafe against the frame, causing a short circuit and potential fire.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V126000·2013-04-09

    Blue Bird Recalls 2008-2011 All American Buses Due to Fire Risk

    Blue Bird is recalling 2008-2011 All American transit buses because a power cable may contact the chassis, causing a short and potential fire.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V134000·2013-04-04

    Altec Recalls 2010-2012 Cranes Due to Outrigger Bracket Defect

    Altec is recalling 2010-2012 AC18, AC23, and AC38 cranes because front bumper outrigger brackets may be inadequate, potentially reducing stability and causing injury or death.

    Product
    ALTEC — ALTEC AC23, AC38, AC18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1257-2013·2013-04-03

    Mkg Provisions Recalls Smoked Salmon Sides Due to Listeria

    Mkg Provisions Inc is recalling Prestige Smoked Scottish Smoked Salmon Sides because a private lab test found Listeria monocytogenes.

    Product
    Prestige Smoked Scottish 2.5-3.5 Smoked Salmon Sides (2-3 lbs.)
    Category
    Food
    Distribution
    2 states