Pink Toyz recalls Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311,…
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an…
Read the official notice →- Date
- 2022-04-27
- Country
- United States
- Brand
- Pink Toyz
- Product
- Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311,…
- Classification
- Class I
- Units
- Nationwide in the USA via walmart.com online marketplace
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2022-04-27
US
Acon Biotech (Hangzhou) Co., Ltd. recalls Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing), CE marked
Non-EUA authorized, CE marked, SARS-CoV-2 antigen rapid test kits are being recalled from the U.S. market because use may lead to inaccurate test results, including false negative or false positive test results.
FDA · DeviceAcon Biotech (Hangzhou) Co., Ltd.US: MD, PA International Distribution to countries of: Hungary and China.Official notice →US
Medtronic Inc recalls Harmony Delivery Catheter System. Part of the Harmony Transcatheter Pulmonary Valve (TPV) Replacement Implantation System.
There is potential for the capsule bond to break during the procedure.
US
Respironics California, LLC recalls Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)), *Distributed outside the United States
Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some cases could result in the ventilator ceasing to operate.
FDA · DeviceRespironics California, LLCWorldwide distribution US Nationwide distribution in the states of AL, AR, AZ,…Official notice →US
VIRGIN SCENT INC recalls artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA…
CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot
US
VIRGIN SCENT INC recalls artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA…
Chemical Contamination: presence of benzene, acetaldehyde, and acetal.
US
North American Custom Laboratories, LLC dba FarmaKeio… recalls PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection, 2mL vials, Rx Only, Farmakeio 1736 N Greenville…
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
FDA · DrugNorth American Custom Laboratories, LLC dba FarmaKeio…Nationwide within United StatesOfficial notice →