Atlas FDA

Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description: Laparosco

FDA device recall Z-2408-2024 · posted 2024-07-17 · Open, Classified

Recall details

Recalling firm
Canadian Hospital Specialties Ltd.
Reason for recall
A customer found product with incomplete seals of P/N 20400161S, lot #185198 which can lead to non-sterile product and patient safety concerns. CHS has validated this complaint.
Action taken
On June 13, 2024 their only direct US consignee was sent an URGENT: MEDICAL DEVICE VOLUNTARY RECALL NOTIFICATION letter. Action to be Taken by the Customer 1. Please acknowledge receipt of this notification by completing the attached Customer Effectiveness Check form. 2. Please notify any customers who have received this product for their awareness. 3. Please notify Canadian Hospital Specialties Ltd. of any remaining affected product in your inventory by completing the Customer Response form along with the Product Destruction Verification form and return via email to Canadian Hospital Specialties Ltd. so credit can be provided. Should you have any questions or concerns, please do not hesitate to reach out to CHS directly at recalls@chsltd.com Monday through Friday from 8:30 am to 4:30 pm Eastern.
Root cause
Under Investigation by firm
Status
Open, Classified
Product code
GCJ
Quantity affected
6300 units
Distribution
US Nationwide distribution in the state of MA.
Date initiated
2024-06-11
Date posted
2024-07-17
Location
Oakville, Canada

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RecordFirmDate
NBS CONNECTING TUBE SET (K001068)Nbs Products CO2000-06-14