The Food and Drug Administration is advising consumers not to purchase or use XXX Zone 40K, a product promoted and sold for sexual enhancement on various websites and possibly in some retail stores.
Similar Posts
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 20 mEq Potassium Chloride Injection Due To Overwrap Mislabeled As 10 mEq Potassium Chloride Injection
FOR IMMEDIATE RELEASE – October 31, 2025 AUSTIN, TX – Otsuka ICU Medical LLC is issuing a voluntary recall to the user level, for a MISLABELLED lot of POTASSIUM CHLORIDE Inj. 20 mEq, NDC 0990-7077-14. The OVERWRAP label of lot 1030613, Expiration Date: 09-30-2026 may incorrectly identify the productPurity Products Announces Recall on the Dietary Supplement, My Bladder Because of Possible Health Risk
Plainview, NY. October 27, 2025— Purity Products is announcing a recall of one lot of of its dietary supplement MyBladder because it has the potential to be contaminated with Escherichia coli O7:K1 and 1303. The presence of these E. coli strains may pose a risk for gastrointestinal or other infectioFDA Modernizes Clinical Trials with Master Protocols
“FDA Modernizes Clinical Trials with Master Protocols” February 26, 2019 IssueNubratori, Inc. Torrance, CA. 483 issued 12/11/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 12/11/2025
Short Title (70 char) Nubratori, Inc. Torrance, CA. 483 issued 12/11/2025
FEI Number 3010166491
Firm Name Nubratori, Inc.
Record Type 483
State CA
Establishment Type Outsourcing FacilityAmish Origins Management, LLC – 704166 – 05/29/2025
CGMP/Finished Pharmaceuticals/AdulteratedPatent Certifications and Suitability Petitions
Information on patents and suitability petitions that impact the availability of generic drugs.
