DeRoyal recalls sterile custom kits with BD PosiFlush syringes due to packaging defects. Affected kits include specific model numbers and lot dates. Consumers should check their kits for the listed serial numbers and contact DeRoyal for details.
DeRoyal manufactured procedure packs using BDPosiFlush syringes which were subsequently recalled due holes in the packaging.
DeRoyal is recalling sterile custom medical kits that were packaged with BD PosiFlush syringes. The recall is due to holes in the packaging, which could lead to contamination or infection risks if the kits are used improperly.
The packaging has holes that could allow contaminants to enter the sterile kits. If the kits are used without proper sealing, this could lead to infections or contamination during medical procedures.
Healthcare professionals and medical facilities that use DeRoyal Sterile Custom Kits with BD PosiFlush syringes are likely affected. Those using the specific model numbers and lot dates listed in the recall are at the highest risk.
Check for model numbers like '89-6209.03' or '89-8748.04' on the kit packaging. Look for lot numbers and expiration dates listed in the recall notice, such as '49935860 exp 4/1/2021' or '51458994 exp 2/1/2022'.
Look for model numbers and lot numbers on the kit packaging to determine if it is affected by this recall.
Reach out to DeRoyal Industries Inc for specific instructions on how to return or replace the affected kits.
The recall is due to holes in the packaging of the sterile custom kits, which could lead to contamination if the kits are used without proper sealing.
Kits with model numbers like '89-6209.03' or '89-8748.04' and specific lot numbers listed in the recall notice are affected.
Check the model number and lot number on your kit packaging against the list provided in the recall notice.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-1963-2020 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-1963-2020 from DeRoyal. 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.
