Custom Healthcare Systems Recalls Little Snipper Circumcision Trays Due to Sterility Compromise
Custom Healthcare Systems is recalling 300 Little Snipper Circumcision Trays because incorrect sealing specifications compromised product sterility.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device where sterility was compromised, creating a risk of infection or harm, but the source text does not report any specific illnesses or injuries, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Custom Healthcare Systems, Inc. is recalling 300 units of the CHS Custom Convenience Kit- LITTLE SNIPPER CIRCUMCISION TRAY, Part Number YMCIR-400. The recall involves Lot Number 61518 with an expiration date of 8/1/2020.
The recall was initiated because the convenience kits were sealed in immediate Tyvek pouches using incorrect specifications, which compromised the sterility of the product. The affected units were distributed to facilities in Connecticut, Georgia, Kentucky, North Carolina, Virginia, Maryland, Oklahoma, Illinois, and South Carolina.
Healthcare facilities and consumers should stop using the affected products immediately and contact Custom Healthcare Systems, Inc. for further instructions or a return.
The recalled product
- Product
- CHS Custom Convenience Kit- LITTLE SNIPPER CIRCUMCISION TRAY Part Number: YMCIR-400
- Manufacturer
- Custom Healthcare Systems, Inc.
- Category
- Medical Device — Surgical Kits
- Affected units
- 300
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number: 61518 Exp. date: 8/1/2020
Distribution
Part of a larger recall action
This product is one of 29 recalled by Custom Healthcare Systems, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 29 products in this recall →Related recalls
Same manufacturer · Custom Healthcare Systems, Inc.
See all →- HighCustom Healthcare Systems Recalls Inpatient Dialysis Kits Due to Latex
FDA (Devices) · 2020-02-05
- HighCustom Healthcare Systems Recalls Penrose Drain Kits Due to Sterility Compromise
FDA (Devices) · 2018-10-31
- HighCustom Healthcare Systems Recalls Suture Removal Kits Due to Sterility Compromise
FDA (Devices) · 2018-10-31
- HighCustom Healthcare Systems Recalls Convenience Kits Due to Sterility Compromise
FDA (Devices) · 2018-10-31
- HighCHS Custom Convenience Kits Recalled for Sterility Compromise
FDA (Devices) · 2018-10-31
Same hazard · sterility compromise
See all →- SevereSpectra Medical Devices Recalls Sodium Chloride Injection Ampules Due to Sterility Concerns
FDA (Devices) · 2026-08-19
- HighStryker Recalls Ahto Dual Spike Tube Set Due to Leaking Handpiece
FDA (Devices) · 2026-08-12
- HighIntramedullary Bone Saw Blade Assembly Recalled Due to Potential Sterile Barrier Damage
FDA (Devices) · 2026-08-12
- ModerateIntramedullary Bone Saw Blade Assembly Recalled Due to Potential Sterile Barrier Damage
FDA (Devices) · 2026-08-12
- HighIntramedullary Bone Saw Blade Assemblies Recalled Due to Potential Packaging Damage
FDA (Devices) · 2026-08-12