Hobbs Medical, Inc. is recalling 367 Posi-Stop Injection Needles because manufacturing debris found inside the device can block the needle's tip. This defect prevents injection solutions from flowing through the needle as intended during medical procedures. The recall affects 23-gauge and 25-gauge needles across nine different catalog models. To date, no incidents or injuries have been reported related to this issue.
Debris from the manufacturing process may be trapped within the needle's inner sheath, causing a complete or partial blockage. If a needle is blocked during use, a patient might not receive their required dose of medication, and there is a potential risk that debris could be introduced into the patient's body.
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
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