American Contract Systems recalls Convenience Kit D & C PACK (LLPD90H) due to catheters not meeting performance specs. Affected units sold with lot code 70-054952.
The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications.
American Contract Systems is recalling their Convenience Kit D & C PACK (model LLPD90H) because samples of the catheters inside didn't meet safety standards. This could mean the catheters might not work properly, which could cause injury during use.
The catheters in the kit may not meet safety standards, which could lead to improper function during medical procedures. This might cause injury if the catheters don't work as intended.
People who bought the Convenience Kit D & C PACK (model LLPD90H) with lot code 70-054952 are affected. Healthcare workers using these catheters for medical procedures are most at risk.
Check for the model number LLPD90H on the kit. Look for lot code 70-054952 on the packaging or label. The kit was sold with this specific lot code.
Look for model number LLPD90H and lot code 70-054952 on the kit packaging.
Medline Industries, LP identified that representative samples of the catheters in the kit did not meet applicable performance specifications.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model and lot code.
The recall states the catheters may not meet performance specs, but does not mention specific injury risks. The hazard level is low risk.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-3003-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-3003-2026 from American Contract Systems. 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.
