Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada Orthopedic 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Orthopedic 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.
Brand
Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
SLIM Handle with Catalog #SLM-HND100 with etched lot code #B204-1 on the handle and with Lot# B204-01 on the packaging label.
Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada is recalling Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Prod due to The lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label.
Recommended Action
Per FDA guidance
On 04/03/2020 Pega Medical Inc. sent out an email which included a Field Safety Notice letter to their US consignee identifying the problem, the actions to be taken by the customer/user in order to prevent risks for patients/users, and the actions planned by Pega Medical Inc. to correct the problem. PRODUCTS: The Handle of the Driver of the Simple Locking intramedullary System (SLIM) WITH CATALOG # SLM-HND100 which was distributed to the identified US consignee on 12/24/2019, with lot #8204-1 marked on the part (the driver handle) and with packaging labeled with lot# 8204-01. ACTION TO BE TAKEN BY THE CUSTOMER/USER: "Identify the device with the same catalogue number and lot number "Verify and correct any record on your files that may indicate the lot number of this part. The lot indicated in the records must be 8204-1. "If the part is still in its original package: Place provided label over the previous label making sure that all the information in the previous label is completely hidden. "If the part is not in its original package: No further action is required.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026