Recall Register

Device recall: Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The…

Class III FDA enforcement event 85531. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

The lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label.

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

Pega Medical Inc. started this device recall on 3 Apr 2020. The firm address in the FDA record is in Laval. FDA put the recall in Class III. FDA event 85531 has 1 product record. The first FDA enforcement report date is 27 May 2020. The record gives the status Terminated, with the termination date 20 Nov 2020.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

US Nationwide Distribution including in the states of Florida. No Foreign Consignees listed.

Recalling firm

Pega Medical Inc., Laval, N/A, Canada.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 85531: product records
Recall numberProductQuantityClassStatusReport date
Z-2038-2020Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.3 unitsClass IIITerminated27 May 2020

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Device events that started in 2020
916
Share of these events in Class III
3%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
9

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 85531. https://recallregister.com/fda/iii/85531/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: US Nationwide Distribution including in the states of Florida. No Foreign Consignees listed.
What quantity of product is in FDA event 85531?
The FDA record gives this quantity: 3 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2020 have the same class?
3% of the 916 device events that started in 2020 are in Class III.