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Open, Classified

Paragon 28, Inc. System: Baby Gorilla/Gorilla Plating System, Ref: P99-100-2816, Material: Stainless Steel; Desc: Drill, 2.4 X 160mm

FDA Recall Z-1458-2022 · Posted None

Recalling FirmParagon 28, Inc.
Recall StatusOpen, Classified
Product CodeHRS
Date Initiated2022-05-18
Product Quantity3 units

Reason for Recall

Incorrect labeling; There is potential that the drill packaging contains the incorrect part number.

Firm Action

Initial communication was made on May 18, 2022 via E-Mail to inform the consignee about the recall. On June 10, 2022, a "Urgent Medical Device Recall" notice was sent via E-mail to affected consignee. Paragon 28 asked the consignee to take the following actions: 1. Review physical inventory of product in your control or at a hospital/health care facility within your region and any affected product that is identified, discontinue use, quarantine and do not distribute any further. 2. Complete the attached Medical Device Recall Response form and return to [email protected]. 3. Return affected devices immediately using the provided return label (attached) and include a copy of the Medical Device Recall Response form. Paragon28, Attn: Recalls 14445 Grasslands Dr. Englewood, CO 80112 4. Report any adverse reactions or quality problems experienced with the use of this product to Paragon 28 ([email protected]), or directly the FDA s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Root Cause

Under Investigation by firm

Distribution Pattern

International distribution in the country of UK.

Official Source

View FDA Recall →

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

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