Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Brand
Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada
Lot Codes / Batch Numbers
Lot # 150115-09, 160427-01 and A162-02
Products Sold
Lot # 150115-09, 160427-01 and A162-02
Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada is recalling SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System due to Handle could jam with the Driver due to the detachment of an internal Connector Ring.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Handle could jam with the Driver due to the detachment of an internal Connector Ring.
Recommended Action
Per FDA guidance
An e-mail was sent on May 25, 2019 to all their consignees with the following instructions. Identify the device with the same catalogue number and lot number and return the device to Pega Medical Inc. as soon as possible to the address shown below using the FedEx Account number provided. Contact Enrique Garcia at (450) 688-5144 ext. 242 or egarcia@pegamedical.com for more information
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 noticeDistribution
As reported by FDA
CA, DE, FL, IL, NE, NY, NC, TN
Page updated: Jan 10, 2026