Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 (Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa) – there is the potential for extended l... (2025)
This recall may present a risk under certain conditions.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Brand
Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa
Lot Codes / Batch Numbers
UDI: (01)00607915126582, Lot # 1546141
Products Sold
UDI: (01)00607915126582; Lot # 1546141
Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa is recalling Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 due to There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Recommended Action
Per FDA guidance
On December 11, 2025, Applied Medical issued a Urgent Medical Device Recall Notification to affected consignees via Email. Applied Medical ask consignees to take the following actions: 1. Check your inventory for recalled product. 2. Quarantine any product from the impacted lot. 3. Complete the attached Customer Recall Notification Confirmation Form. Please note that you must return the form even if you have no devices in inventory. 4. Please notify any facilities to which you distributed the affected product with a copy of this notification. Please also complete the Distributor Recall Notification Confirmation Report. 5. Return the Recall Notification Confirmation Form to Applied Medical by emailing to removal60924496@appliedmedical.com 6. Return affected product and a copy of the Recall Notification Confirmation Form to Applied Medical
Verify this information on the official source
This page aggregates publicly available data. Always confirm recall details directly with the U.S. Food and Drug Administration (FDA) before taking action.
View official FDA recall noticeDistribution
As reported by FDA
CA, ME, MI
Page updated: Jan 10, 2026
Important Notice
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