Hobbs Medical recalls Posi-Stop Injection Needles with incorrect expiration dates that extend shelf life. Affected units sold from March 2018 to September 2020 with specific lot numbers.
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)
Hobbs Medical is recalling Posi-Stop Injection Needles that have incorrect expiration dates, which extends their shelf life beyond the intended period. This could lead to using needles that are no longer safe or effective after their intended expiration date.
The needles have an incorrect expiration date label that extends the shelf life of the product. This means the needles may be used beyond their intended expiration date, potentially leading to reduced effectiveness or safety issues.
Users of the Hobbs Posi-Stop Injection Needles with lot numbers ending in 'R' or kits containing at least one such needle are affected. Healthcare professionals and patients using these needles for medical injections are most at risk.
Check the lot number on the needle packaging; affected units have lot numbers ending in 'R'. The product was distributed in the United States from March 25, 2018, to September 28, 2020.
Look for lot numbers ending in 'R' on the packaging or product label.
The recall record does not specify the correct expiration date.
Check the lot number on the packaging; affected units have lot numbers ending in 'R'.
The recall record does not mention a return or remedy action.
We’ve drafted a message you can send Hobbs Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0025-2023 — Hobbs Medical Hobbs Medical Hello, I own a Hobbs Medical that is covered by recall Z-0025-2023 from Hobbs Medical. 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.
