Use caution Medical device recall · FDA · Published August 10, 2026

Medical Convenience Kits with Contaminated Wipes Risk Infection

American Contract Systems recalls 1,804 medical convenience kits containing BD CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant, increasing risk of skin irritation or infection.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-3294-2026Medical device American Contract Systems ›

Use caution until it’s fixed

Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).

✎ GovInfoNow plain-language explainer

American Contract Systems recalls 1,804 medical convenience kits that contain BD CliniClean Pericare Wipes which may be contaminated with a lubricant used during manufacturing. Using these contaminated wipes could cause skin irritation or increase the risk of urinary tract infections. Read more at govinfonow.com/recall/1449399-american-contract-systems-inc-recalls-medical-convenience-kits-containing-bd.

Source Summary by GovInfoNow · govinfonow.com/recall/1449399-american-contract-systems-inc-recalls-medical-convenience-kits-containing-bd · Updated October 14, 2026 · FDA enforcement record: FDA #Z-3294-2026

Cite this page

“Medical Convenience Kits with Contaminated Wipes Risk Infection.” GovInfoNow, updated October 14, 2026. https://govinfonow.com/recall/1449399-american-contract-systems-inc-recalls-medical-convenience-kits-containing-bd. Based on FDA recall #Z-3294-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3294-2026%22&limit=1).

The FDA announced on 2026-08-10 that American Contract Systems Inc is recalling 1,804 medical convenience kits containing contaminated BD CliniClean Pericare Wipes. The hazard involves potential skin irritation or increased infection risk from lubricant contamination.

How to tell if you have it

Brand: American Contract Systems
Product: Medical Convenience Kits
Model No. MHAH55AM, UDI-DI 191072236487, Lots 42-8529911 through 42-8869711
Model No. SPLL54U, UDI-DI 191072239181, Lots 07-2516111 through 07-2561411
Model No. SPVH62P, UDI-DI 191072238771, Lots 07-2544611 and 12-7436711

The hazard

The kits contain manufacturer-recalled perineal care wipes contaminated with a lubricant used during manufacturing. Use of these wipes may cause localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of the contaminated wipes may increase the risk of localized infection or catheter-associated urinary tract infection (CAUTI).

Context

GovInfoNow's records show American Contract Systems Inc has 21 other recalls on record since 2018-11-21. Other recent recalls include a 2026-06-29 recall for catheters that may not meet performance standards and a 2026-05-19 recall for medical kits with potential endotoxin variability. Similar recent recalls of contaminated wipes include Cardinal Health Presource Packs recalled on 2026-07-29.

How to tell if you have this one

Look for kits with model numbers MHAH55AM, SPLL54U, or SPVH62P. Check for lot numbers 42-8529911, 42-8649211, 42-8687711, 42-8797811, 42-8857011, 42-8869711 or 07-2516111, 07-2528611, 07-2545611, 07-2547911, 07-2561411, 07-2544611, 12-7436711.

Brand
American Contract Systems
Category
Medical device

FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution in the states of Iowa, Minnesota, Wisconsin, and South Dakota.

Recall number	Product, codes & lots
Z-3292-2026	Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ROBOTIC PACK - 242561 Model No. MHRB88AO; UDI-DI 191072236531 Lots 42-8513411 42-8580011 42-8663211 42-8775711 42-8801311 42-8840611 42-8865911
Z-3293-2026	Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays CARDIAC HEART BUNDLE NS Model No. LMCH99P OPEN HEART 2 RCH¿ 0248495 Model No. RCOH62C; LMCH99P UDI-DI 191072228147 Lots 42-8533511 42-8669111 42-8763811 42-8811311 42-8825411 42-8869411 RCOH62C UDI-DI 191072230942 Lots 42-8504411 42-8561511 42-8668211 42-8737811 42-8797911 42-8862511
Z-3294-2026	Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989 Model No. MHAH55AM LAVH-LAP COLON Model No. SPLL54U VAG HYST PACK Model No. SPVH62P; MHAH55AM UDI-DI 191072236487 Lots 42-8529911 42-8649211 42-8687711 42-8797811 42-8857011 42-8869711 SPLL54U UDI-DI 191072239181 Lots 07-2516111 07-2528611 07-2545611 07-2547911 07-2561411 SPVH62P UDI-DI 191072238771 Lots 07-2544611 12-7436711

Based on the official FDA remedy

What to do — step by step

Check Kit Model
Identify the model number on the kit (MHAH55AM, SPLL54U, or SPVH62P) to determine if it's affected.
Verify Lot Number
Check the lot number on the kit (42-8529911, 42-8649211, 42-8687711, 42-8797811, 42-8857011, 42-8869711, 07-2516111, 07-2528611, 07-2545611, 07-2547911, 07-2561411, 07-2544611, 12-7436711) to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 4 states.

FDA distribution: “US Nationwide distribution in the states of Iowa, Minnesota, Wisconsin, and South Dakota.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Iowa, Minnesota, South Dakota, Wisconsin.

Recall timeline

FDA published this recall 58 days after the firm started it.

Aug 10, 2026Firm started the recall
Sep 25, 2026FDA classified it Class II
Oct 7, 2026Published in FDA’s Enforcement Report
Oct 13, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/1449399-american-contract-systems-inc-recalls-medical-convenience-kits-containing-bd">Medical Convenience Kits with Contaminated Wipes Risk Infection (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-3294-2026 (August 10, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3294-2026 to see it in context.
Plain-language summary written by qwen3:4b on October 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.