Cadence Science recalls glass syringes that may break during use, posing a risk of injury. Affected models include Part Nos. 5338-5343 with specific GTINs. Consumers should stop using and contact for replacement.
The glass syringe used with Pressure Control Syringes may potentially break during use.
Cadence Science is recalling glass syringes that could break during use, potentially causing injury. This recall affects specific model numbers sold in hospitals and medical settings. The risk is real but not immediate for all users.
The glass syringe used with Pressure Control Syringes may break during use, which could lead to injury from sharp fragments or sudden release of pressure. This risk is higher in medical settings where precise handling is required.
Healthcare professionals and hospital staff who use these syringes are most at risk. Patients receiving treatments with these syringes may also be affected if the device breaks.
Check for Part Numbers 5338, 5339, 5340, 5341, 5342, or 5343 with the listed GTINs. These syringes are used in hospitals and medical settings, so look for them in hospital equipment catalogs.
Discontinue use of the glass syringe if it is part of the recalled models to prevent potential breakage.
Reach out to Cadence Science for a replacement or refund as the recall does not specify a replacement process.
The glass syringe used with Pressure Control Syringes may break during use, which could cause injury.
Part Nos. 5338, 5339, 5340, 5341, 5342, and 5343 with specific GTIN numbers listed in the recall.
Yes, but the recall does not specify a replacement process; contact Cadence Science directly for assistance.
We’ve drafted a message you can send Cadence Science to request your refund or repair — edit it as you like.
Subject: Recall Z-0365-2020 — Cadence Science Cadence Science Hello, I own a Cadence Science that is covered by recall Z-0365-2020 from Cadence Science. 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.
