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Terminated

Port full Access Tray Product Code: DT19330

FDA Recall Z-0253-2020 · Posted None

Recalling FirmCenturion Medical Products Corporation
Recall StatusTerminated
Product CodeLRP
Date Initiated2019-07-15
Date Terminated2020-08-31
Product Quantity240 kits

Reason for Recall

Supplier initiated recall of the GRIPPER Needles

Firm Action

1. Please identify all inventory that you have within your possession and cease use immediately. 2. Complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter. Upon receipt of this record, Centurion Representative will contact you regarding retrieval of the product from your facility. 3. Please forward this recall information to any facilities to who this product may have been further distributed, instructing them to cease use immediately.

Root Cause

Nonconforming Material/Component

Distribution Pattern

IL

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K021999GRIPPER PLUS NEEDLEDeltec, Inc. · 2002-08-13

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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