American Contract Systems recalls
10 recent recalls on record for American Contract Systems in connected official government data as of October 22, 2026 at 12:00 PM UTC.
Models with recalls
All American Contract Systems recalls
FDA Class II · Medical device · October 7, 2026
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Official ID Z-3294-2026 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Official ID Z-3293-2026 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. U…
Official ID Z-3292-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Official ID Z-3003-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Official ID Z-3002-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Official ID Z-3001-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Official ID Z-3000-2026 ·
Official record ↗
FDA Class II · Medical device · August 26, 2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…
Official ID Z-2990-2026 ·
Official record ↗
FDA Class II · Medical device · August 26, 2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…
Official ID Z-2989-2026 ·
Official record ↗
FDA Class I · Medical device · May 13, 2026
Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between …
Official ID Z-1981-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.