American Contract Systems recall: Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary…
American Contract Systems Inc is recalling Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary… – 1,804 kits total. The U.S. Food and Drug Administration published the recall on October 7, 2026; it began on August 10, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary… |
| Brand | American Contract Systems |
| Company | American Contract Systems Inc |
| Type | Medical devices |
| Classification | Class II |
| Recall date | August 10, 2026 |
| Published by FDA | October 7, 2026 |
| Quantity | 1,804 kits total |
| Recall ID | 99759 |
Recalled products (3)
- Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ROBOTIC PACK - 242561 Model No. MHRB88AO
- FDA recall number
- Z-3292-2026
- Codes, lots and dates
- UDI-DI 191072236531 Lots 42-8513411 42-8580011 42-8663211 42-8775711 42-8801311 42-8840611 42-8865911
- Quantity
- 1,804 kits total
- Classification
- Class II
- 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
- FDA recall number
- Z-3293-2026
- Codes, lots and dates
- 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
- Quantity
- 1,804 kits total
- Classification
- Class II
- 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
- FDA recall number
- Z-3294-2026
- Codes, lots and dates
- 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
- Quantity
- 1,804 kits total
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99759
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Tiffin, OH, United States
Why it was recalled
The reason the FDA lists: “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).”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the states of Iowa, Minnesota, Wisconsin, and South Dakota.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99759, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other American Contract Systems recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 2, 2026 |  American Contract Systems recall: American Contract System Convenience Kit and 1 more productMedical devices · 30 units; 12 units | The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and R… Serious | FDA Class II |
| Aug 26, 2026 | American Contract Systems recall: Medical procedure kits and trays labeled as: 1) CRANI PACK and 1 more productMedical devices · 4789 kits; 160 kits | a sterility problem Serious | FDA Class II |
All 3 American Contract Systems recalls →
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| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is American Contract Systems Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary… recalled?
Yes. American Contract Systems Inc recalled it on August 10, 2026; FDA published it October 7, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
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).
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.