Drugs & medicalClass II

New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy…

Lack of Assurance of Sterility

Read the official notice →
Date
2021-10-06
Country
United States
Brand
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy
Product
Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy 4139 Cadillac Ct # 201…
Classification
Class II
Units
Nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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 New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls

  1. 2023-08-02
  2. US
    Drugs & medicalClass II

    New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed oil, Compounded Rx, For…

    Lack of Assurance of Sterility

    FDA · DrugNew Vitalis Pharmacy LLC dba New Vitalis PharmacyNationwideOfficial notice →
All 2 New Vitalis Pharmacy LLC dba New Vitalis Pharmacy recalls →

Other drugs & medical recalls in the United States

  1. 2021-10-06
  2. US
    Drugs & medicalClass I

    Accelerated Care Plus Corporation recalls Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound…

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue:…

    FDA · DeviceAccelerated Care Plus CorporationUS nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass I

    Deroyal Industries, Inc. Lafollette recalls DeRoyal Procedure Packs containing Smiths Medical NORMOFLO Irrigation Warming Set

    DeRoyal manufactured procedure packs containing a Smiths Medical NORMOFLO Irrigation Warming System which is recalled due to the potential for aluminum ions leaching into warming fluids.

    FDA · DeviceDeroyal Industries, Inc. LafolletteUS distribution in Florida and South Carolina.Official notice →
  4. US
    Drugs & medicalClass II

    Greiner Bio-One North America, Inc. recalls VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

    Blood collection tubes may experience a clotting issue.

    FDA · DeviceGreiner Bio-One North America, Inc.Distribution was made to AL, AZ, CO, CT, FL, IL, MA, MD, MI, MO, NC, NM, PA,…Official notice →
  5. US
    Drugs & medicalClass II

    SigmaPharm Laboratories LLC recalls Sodium Phenylbutyrate Powder, 250 Grams, Rx Only, packaged in 500 cc HDPE bottles and 53 mm CRC caps packed in a carton and then in…

    Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.

    FDA · DrugSigmaPharm Laboratories LLCNationwideOfficial notice →
  6. US
  7. US
    Drugs & medicalClass II

    Washington Homeopathic Products, Inc. recalls Occular Allergy Blend 87% Alcohol; In Equal Parts of Apis Mellifica 7x Allium Cepa 7x Euphrasia Officinalis 7X Sabadilla…

    Out-of-specification test results obtained for identification testing based on HPTLC analysis.

    FDA · DrugWashington Homeopathic Products, Inc.Distributed Nationwide in the USAOfficial notice →
See all drugs & medical recalls →