Promaderm Ltd. is recalling 4,754 units of various Mesoram medical devices, including multi-injectors and hypodermic needles, because they may not have been properly sterilized despite being labeled as sterile. These devices are used in veterinary mesotherapy procedures. While no injuries or incidents have been reported to date, using non-sterile medical equipment can lead to serious infections in animals.
The lack of sterility in these injection devices means they may be contaminated with bacteria or other pathogens. When used to perform injections, these contaminants can be introduced directly into an animal's tissue, potentially causing localized or systemic infections.
You have 2 options:
Recall #: V-0035-2022; Quantity: 550 units
Recall #: V-0036-2022; Quantity: 72 units
Recall #: V-0037-2022; Quantity: 36 units
Recall #: V-0038-2022; Quantity: 36 units
Recall #: V-0039-2022; Quantity: 1548 units
Recall #: V-0040-2022; Quantity: 2124 units
Recall #: V-0041-2022; Quantity: 108 units
Recall #: V-0042-2022; Quantity: 108 units
Recall #: V-0043-2022; Quantity: 72 units
Recall #: V-0044-2022; Quantity: 100 units
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response