Drugs & medicalClass II

Pharmacy Plus, Inc. dba Vital Care Compounder recalls MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only, Vital Care Compounder, 115 S. 40th Ave.,…

Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

Read the official notice →
Date
2022-11-09
Country
United States
Brand
Pharmacy Plus, Inc. dba Vital Care Compounder
Product
MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
Classification
Class II
Units
AL, LA, MS, and TN
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Pharmacy Plus, Inc. dba Vital Care Compounder recalls

  1. 2023-04-26
  2. US
All 2 Pharmacy Plus, Inc. dba Vital Care Compounder recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-09
  2. US
  3. US
    Drugs & medicalClass II

    Edwards Lifesciences, LLC recalls Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP 120807FP Fogarty…

    Due to an increase of confirmed latex deterioration complaints for arterial embolectomy catheters packaged in pouches.

    FDA · DeviceEdwards Lifesciences, LLCWorldwide distribution - U.S. Nationwide distribution including in the states…Official notice →
  4. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa Bed, Product Code/Part Number P00697903.

    Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/doppler, infusion pumps, and insulin…

    FDA · DeviceBaxter Healthcare CorporationUSOfficial notice →
  5. US
    Drugs & medicalClass III

    Genentech Inc recalls Susvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susvimo single-dose vial and One Susvimo initial fill…

    Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.

    FDA · DrugGenentech IncNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles, Rx only, Distributed by: Sun Pharmaceutical…

    Presence of Foreign Substance

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide with the United StatesOfficial notice →
  7. 2022-11-02
  8. US
    Drugs & medicalClass II

    Wright Medical Technology, Inc. recalls Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3

    The tibial tray lock detail is oversized (larger than specification).

    FDA · DeviceWright Medical Technology, Inc.US Nationwide distribution in the state of New York.Official notice →
See all drugs & medical recalls →