Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Hobbs Medical, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0472-2025 — Hobbs Medical, Inc. Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Numbe Hello, I own a Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721 that is covered by recall Z-0472-2025 from Hobbs Medical, Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
