The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. 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.

7601–7625 of 29121

  • SevereFDA (Drugs)·D-0111-2022·2021-11-17

    Estradiol Valerate Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Estradiol Valerate 30 mg/mL Injectable due to lack of assurance of sterility. The product was distributed across the United States, Washington, D.C., and Puerto Rico.

    Product
    ESTRADIOL VALERATE 30MG/ML INJ #1 IN ETHYL OLEATE OIL INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0141-2022·2021-11-17

    Talon Compounding Pharmacy Quad-Mix Injectable Lacks Sterility Assurance

    Talon Compounding Pharmacy is recalling a compounded injectable medication (Quad-Mix) due to lack of assurance of sterility. The product was distributed across the United States, Washington D.C., and Puerto Rico.

    Product
    QUAD-MIX PAPAV 30/PHENTOL 3/PGE-1 100/ATROPINE 0.2 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0154-2022·2021-11-17

    Talon Compounding Pharmacy Injectable Sterility Recall

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Test Cypionate 200mg/Anastrozole 0.5mg/Dutasteride 1mg/ml injectable (4 vials) due to lack of assurance of sterility.

    Product
    TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1MG/ML #2 INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0098-2022·2021-11-17

    Injectable Diet Aid Product Recalled for Sterility Assurance Failure

    Talon Compounding Pharmacy is recalling Well's Lipo-Lean injectable vials (Lot 08062021:30) due to lack of assurance of sterility. The product is distributed across the United States, Washington D.C., and Puerto Rico.

    Product
    (WELL'S LIPO-LEAN)INOSITOL/CHOLINE/B-COMP+LEUCINE+CARN+ CHROM+LIDO 25MG/25MG/1.5MG/25MG/25MCG/10MG INJECTABLE in vials, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0146-2022·2021-11-17

    Talon Compounding Pharmacy Injectable Lacks Sterility Assurance

    Talon Compounding Pharmacy is recalling TRIMTROPIC injectable due to lack of assurance of sterility. The affected lot was distributed across the United States, Washington, D.C., and Puerto Rico.

    Product
    TRIMTROPIC - MIC B COMPLEX/CHROM/CARN 20MG/40MG/50MG/5MG/33MG/2MG/1MG/25MCG/25MG INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0186-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable Recalled Due to Sterility Assurance Failure

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.25/PGE-1 6 injectable vials due to lack of assurance of sterility. The injectable medication was distributed across the United States, including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.25/PGE-1 6 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0193-2022·2021-11-17

    TRI-MIX PAPAVERINE Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 20/PHENTOLAMINE 1/PGE-1 20 injectable due to lack of assurance of sterility. The product was distributed in the United States including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 20/PHENTOLAMINE 1/PGE-1 20 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0121-2022·2021-11-17

    Talon Compounding Pharmacy IVME SUPER B Injectable Recalled for Sterility Assurance

    Talon Compounding Pharmacy is recalling IVME SUPER B Injectable vials due to lack of assurance of sterility. The recall affects vials distributed across the United States.

    Product
    IVME SUPER B INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0188-2022·2021-11-17

    Tri-Mix Papaverine Injection Recalled Due to Sterility Assurance Lack

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine 15/Phentolamine 1/PGE-1 10 injectable vials due to lack of assurance of sterility. The affected lot (09082021:40, BUD 02/08/2022) was distributed throughout the United States including Washington, D.C. and Puerto Rico.

    Product
    TRI-MIX PAPAVERINE 15/PHENTOLAMINE 1/PGE-1 10 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0132-2022·2021-11-17

    MIC B12 and L-Carnitine Injectable Recalled for Lack of Sterility Assurance

    Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling MIC B12 25/50/50/0.5MG/ML L-Carnitine 250MG/ML Injectable due to lack of assurance of sterility. The product was distributed across the United States, Washington, D.C., and Puerto Rico.

    Product
    MIC B12 25/50/50/0.5MG/ML L-CARNITINE 250MG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·21V886000·2021-11-16

    Jayco Recalls 2020-2022 Motorhomes Due to Rear Suspension Fastener Defect

    Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, ANTHEM, REATTA, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·044-2021·2021-11-15

    Shamrock Foods Recalls Raw Ground Beef Patties Due to Plastic Contamination

    Shamrock Foods is recalling approximately 6,876 pounds of raw ground beef patties because they may contain pieces of hard, white plastic.

    Product
    Shamrock Foods Company — Shamrock Foods Company DBA Gold Canyon Meat Company Recalls Raw Ground Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V876000·2021-11-12

    2021-2022 Continental Cargo and Cargo Mate Trailers: Welding Defect in Coupler

    Forest River is recalling certain 2021-2022 Continental and Cargo Mate cargo trailers due to an improperly welded coupler. The defect may cause the trailer to separate from the tow vehicle, increasing crash risk.

    Product
    CARGO MATE — CARGO MATE, CONTINENTAL CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V882000·2021-11-12

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc and increasing fire risk.

    Product
    WESTERN STAR — WESTERN STAR 4900, 5700, 4700, 6900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V881000·2021-11-12

    Volvo Recalls 2021 XC40 BEV Vehicles Due to Loose Engine Bolt

    Volvo is recalling 2021 XC40 BEV vehicles because a bolt securing the electrical motor bracket may be loose or missing, which could reduce structural protection in a crash.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V878000·2021-11-12

    Alfa Romeo Stelvio and Giulia fuel line sensor housing cracks

    The fuel line sensor housing in certain 2020-2021 Alfa Romeo Stelvio and Giulia vehicles may crack and leak fuel, causing engine stalls and increasing fire risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V880000·2021-11-12

    Chrysler Recalls 2019-2020 Ram Trucks for Fuel Pump Failure Risk

    Chrysler is recalling 2019-2020 Ram trucks with Cummins 6.7L diesel engines because the high-pressure fuel pump may fail, causing sudden engine stalls that increase crash risk.

    Product
    RAM — RAM 5500, 2500, 4500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E094000·2021-11-12

    Chrysler Recalls Mopar High Pressure Fuel Pumps and 6.7L Engines

    Chrysler is recalling specific Mopar High Pressure Fuel Pumps and 6.7L Cummins Turbo Diesel Engines because the pump may fail, causing the engine to stall without warning.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0119-2022·2021-11-10

    Monoject Prefilled Syringe Plunger Defect Recall: Air Reintroduction Risk

    Monoject prefilled syringes in medical kits may have a plunger that rebounds after air expulsion, potentially reintroducing air into the syringe. This FDA Class I recall affects approximately 9,378 units distributed in Florida and Pennsylvania.

    Product
    Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical Solutions Custom Convenience Kits: AMS-9041CP Leaderflex Insertion Kit with Ultrasound, AMS-9046CP-1 Insertion Tray-RX, AMS8939A Universal Procedure Pack w/Sp
    Category
    Medical Device
    Distribution
    2 states
  • SevereUSDA FSIS·043-2021·2021-11-10

    Innovative Solutions Recalls Chicken Patties Due to Possible Bone Contamination

    Innovative Solutions, Inc. is recalling raw chicken patty products that may contain pieces of bone. No illnesses have been reported.

    Product
    Innovative Solutions, Inc — Innovative Solutions, Inc. Recalls Chicken Patty Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V873000·2021-11-10

    Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect

    The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND WAGONEER, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide