SunMed recalls Full Kit Pulset 3cc Syringes with non-sterile spare needles that could cause skin infections or sepsis if used. Affected units include specific lot numbers and reference codes.
The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.
SunMed is recalling syringes that contain non-sterile needles, which could lead to skin infections or sepsis if used. This is a serious risk for anyone using the syringes for medical injections.
The spare needle in the syringes is not sterile, meaning it could introduce harmful bacteria into the body. If the needle is used on skin, it might cause infections or sepsis, a severe bloodstream infection.
People who own or use the recalled syringes, especially those administering injections to themselves or others. Those with medical conditions requiring frequent injections are at higher risk.
Check for the product name 'Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH' with REF Number 3373-91. Look for lot numbers 010822N23, 052521N54, 081821N05, or 101221N11 on the label.
Immediately stop using the recalled syringes as they contain non-sterile needles that could cause infections.
The syringes contain non-sterile spare needles that could lead to skin infections or sepsis if used.
Lot numbers 010822N23, 052521N54, 081821N05, and 101221N11 are affected.
Check for the product name 'Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH' with REF Number 3373-91 and the listed lot numbers.
We’ve drafted a message you can send SunMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1779-2022 — SunMed SunMed Hello, I own a SunMed that is covered by recall Z-1779-2022 from SunMed. 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.
