Drugs & medicalClass II

Astral SteriTech Private Ltd. recalls Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC…

Lack of Assurance of Sterility

Read the official notice →
Date
2023-05-24
Country
United States
Brand
Astral SteriTech Private Ltd.
Product
Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2023-05-24
  2. US
    Drugs & medicalClass I

    ICU Medical Inc recalls Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010

    Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the…

    FDA · DeviceICU Medical IncworldwideOfficial notice →
  3. US
    Drugs & medicalClass I

    Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351

    Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

    FDA · DeviceDraeger Medical, Inc.Domestic: US Nationwide Distribution.Official notice →
  4. US
  5. US
  6. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Ketotifen Fumarate 0.025 %, Antihistamine eye drops, 5mL bottle, MFG: Akorn, Lake Forrest IL 60045, Repackaged by: RemedyRepack Inc.,…

    CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.

    FDA · DrugRemedyRepack Inc.Product was distrituded to three direct account in PA.Official notice →
  7. US
    Drugs & medicalClass II

    Sanofi-Aventis U.S. LLC recalls Admelog, insulin lispro injection, 100 units/mL (U-100), 3mL multi-dose vial, Rx Only, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807 A…

    Lack of Assurance of Sterility: Malformed crimped collar seal

    FDA · DrugSanofi-Aventis U.S. LLCNationwide in the USAOfficial notice →
See all drugs & medical recalls →