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.

21576–21600 of 32121

  • SevereFDA (Drugs)·D-0066-2016·2015-11-04

    FDA Recalls Compounded Chorionic Gonadotropin Syringes Due to Sterility Concerns

    FDA is recalling 42 syringes of compounded chorionic gonadotropin from Moses Lake Professional Pharmacy due to lack of assurance of sterility.

    Product
    CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 150 UNITS/0.150 ML per syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0097-2016·2015-11-04

    Trader Joe's Coconut Cranberry Granola Recalled for Undeclared Allergens

    New England Natural Bakers is recalling Trader Joe's Coconut Cranberry Granola because it may contain undeclared milk, wheat, and pecans.

    Product
    Trader Joes Coconut Cranberry Granola (SKU 51131), packaged in a 16 oz. box, with Best By date 08/19/16 printed at the top of the package UPC Code: 0051 1315 printed on side panel.
    Category
    Food
    Distribution
    19 states
  • SevereFDA (Drugs)·D-0117-2016·2015-11-04

    FDA Recalls Compounded Progesterone Pellets Due to Sterility Concerns

    JD & SN Inc. is recalling compounded progesterone pellets because the agency cannot ensure they are sterile. Consumers should stop using the product and contact their healthcare provider.

    Product
    PROGESTERONE, Pellet, 200 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0153-2016·2015-11-04

    Moses Lake Pharmacy Recalls Vitamin B-Complex Injectable Solution

    JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling Vitamin B-Complex Injectable Solution due to a lack of assurance of sterility.

    Product
    VITAMIN B-COMPLEX, Injectable Solution, Syringe size: 30 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0091-2016·2015-11-04

    Moses Lake Pharmacy Recalls Folic Acid Injectable Solution Due to Sterility Concerns

    JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling six syringes of Folic Acid Injectable Solution because the sterility of the compounded drug cannot be assured.

    Product
    FOLIC ACID, Injectable Solution, 10 mg/mL, 30 mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0103-2016·2015-11-04

    Moses Lake Pharmacy Recalls Methylcobalamin Injectable Solution Due to Sterility Concerns

    JD & SN Inc. is recalling specific syringes of Methylcobalamin injectable solution because the agency could not ensure the product remained sterile.

    Product
    METHYLCOBALAMIN, injectable Solution, 10 MG/ML, syringe sizes: 10mL; 22.5mL; and 30mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0093-2016·2015-11-04

    FDA Recalls Injectable Glutathione Due to Sterility Assurance Concerns

    FDA is recalling 2 syringes of injectable glutathione from Moses Lake Professional Pharmacy because the sterility of the compounded drug cannot be assured.

    Product
    GLUTATHIONE (L), Injectable Solution, 75 mg/mL, 64 mL syringe , Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0191-2016·2015-11-04

    Resource Optimization Recalls Custom Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 10 custom surgical kits distributed in Texas and Louisiana because compromised package integrity may affect sterility.

    Product
    Regard, Item Number 800500002, Sterile, CV0578B - CV PACK- Custom surgical kit for surgery.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0064-2016·2015-11-04

    Moses Lake Pharmacy Recalls Chorionic Gonadotropin Due to Sterility Concerns

    JD & SN Inc. is recalling specific vials of Chorionic Gonadotropin because the FDA cannot assure the sterility of the compounded drug.

    Product
    CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL; 5 mL; 6 mL; 7.5 mL ; 9 mL, 10 mL; 12 mL; 15 mL; 20 mL; 28 mL; Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0140-2016·2015-11-04

    Moses Lake Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns

    JD & SN Inc. is recalling 90 mg testosterone pellets because the agency could not ensure the sterile compounded drugs were sterile.

    Product
    TESTOSTERONE, Pellet, 90 mg, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0142-2016·2015-11-04

    Moses Lake Pharmacy Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    Moses Lake Professional Pharmacy is recalling Testosterone Cypionate for Subcutaneous Injection because the product lacks assurance of sterility.

    Product
    TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 100 mg/mL, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0057-2016·2015-11-04

    FDA Recalls Alprostadil/Procaine Injectable Solution Due to Sterility Concerns

    The FDA is recalling 27 vials of Alprostadil/Procaine Injectable Solution because the manufacturer cannot ensure the product is sterile.

    Product
    ALPROSTADIL/PROCAINE, Injectable Solution, 40 MCG/0.1%/ML, 10 mL and 20 mL vials, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0063-2016·2015-11-04

    FDA Recalls Chorionic Gonadotropin Syringes Due to Sterility Concerns

    The FDA is recalling 834 syringes of Chorionic Gonadotropin compounded by Moses Lake Professional Pharmacy because the agency cannot ensure the product is sterile.

    Product
    CHORIONIC GONADOTROPIN, Injectable Solution,175 UNITS/1.5mg per syringe with Methylcobalamin, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0150-2016·2015-11-04

    Moses Lake Pharmacy Recalls Six Trimix Syringes Due to Sterility Concerns

    JD & SN Inc. is recalling six syringes of Trimix injectable solution because the company cannot guarantee the product's sterility.

    Product
    TRIMIX, injectable Solution, 30MG/1MG/20MCG, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0078-2016·2015-11-04

    FDA Recalls Estradiol Pellets Due to Lack of Sterility Assurance

    JD & SN Inc. is recalling Estradiol pellets because the FDA determined there is a lack of assurance of sterility for all sterile human compounded drugs within their expiry.

    Product
    ESTRADIOL, Pellet, 12.5 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0117-2016·2015-11-04

    American Pure Whey Protein Recalled for Undeclared Soy and Milk Allergens

    American Pure Whey is recalling Whey Protein Matrix Chocolate flavor containers due to undeclared soy and milk allergens.

    Product
    American Pure Whey, Whey Protein Matrix Chocolate flavor, 2 lb. and 5 lb. containers, Manufactured by American Pure Whey, Vanceboro, NC.
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Drugs)·D-0143-2016·2015-11-04

    FDA Recalls Testosterone Cypionate Injection Due to Sterility Concerns

    FDA is recalling Testosterone Cypionate for SubQ Injection from Moses Lake Professional Pharmacy due to lack of assurance of sterility.

    Product
    TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 200 mg/mL, syringe size: 5ml and 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0158-2016·2015-11-04

    Park Compounding Pharmacy Recalls TRI-MIX Vials Due to Sterility Concerns

    Park Compounding Pharmacy is recalling specific lots of TRI-MIX vials because the agency could not ensure the products were sterile.

    Product
    TRI-MIX 10MCG+0.5MG+15MG/ML,5 mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·15V725000·2015-11-03

    Prevost Recalls 2016 Coaches Due to Front Suspension Stud Failure Risk

    Prevost is recalling 2016 H3-45 and X3-45 VIP coaches because front suspension studs may fail, allowing a wheel to turn unexpectedly and increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16025·2015-11-03

    GE Recalls Zoneline Air Conditioners and Heating Units Due to Fire Risk

    GE is recalling about 33,500 Zoneline air conditioning and heating units due to a risk of fire caused by moisture accumulation and electrical arcing.

    Product
    GE Zoneline® Air Conditioners and Heating Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V723000·2015-11-02

    KME Recalls 2016 Predator and Severe Service Vehicles for Axle Defect

    KME is recalling 2016 Predator and Severe Service vehicles because improperly tightened axle hex nuts may cause the driveshaft to disconnect, increasing crash risk.

    Product
    KME — KME SEVERE SERVICE, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V721000·2015-11-02

    Indian Motorcycle Recalls 2015-2016 Models Due to Rear Brake Failure

    Indian Motorcycle is recalling 7,614 motorcycles from 2015-2016 because a rear brake master cylinder defect may cause a loss of braking power.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, CHIEF VINTAGE, CHIEFTAIN, ROADMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V722000·2015-11-02

    Trans Tech School Buses Recalled for Wheelchair Lift Bearing Defect

    Transportation Collaborative is recalling 188 Trans Tech school buses equipped with certain Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure operators.

    Product
    TRANS TECH BUS — TRANS TECH BUS, TRANS TECH STUDENT SAFETY TRANSPORT, ROADSTER, ST AERO, ROADSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·135-2015·2015-11-01

    All American Meats Recalls Ground Beef Due to E. Coli O157:H7 Risk

    All American Meats is recalling approximately 167,427 pounds of ground beef products due to possible E. coli O157:H7 contamination. No illnesses have been reported.

    Product
    All American Meats, Inc. — All American Meats, Inc. Recalls Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide