Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): Medical Device Recall in 2022 - (Recall #: Z-0782-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

LINQ II Insertable Cardiac Monitor

Product Classification:

Class II

Date Initiated: January 18, 2022

Date Posted: March 23, 2022

Recall Number: Z-0782-2022

Event ID: 89469

Reason for Recall:

Devices may lose functionality due to susceptibility to moisture ingress.

Status: Ongoing

Product Quantity: 8 devices

Code Information:

8 impacted devices with the following Serial number and GTIN 1) Serial RLB035341G (GTIN 00763000060374) 2) Serial RLB051224G (GTIN 00763000060374) 3) Serial RLB059666G (GTIN 00763000060374) 4) Serial RLB061064G (GTIN 00763000060374) 5) Serial RLB061812G (GTIN 00763000060381) 6) Serial RLB066367G (GTIN 00763000060374) 7) Serial RLB091638G (GTIN 00763000060374) 8) Serial RLB122769G (GTIN 00763000554002)

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of NJ, NY, PA, and VA. The country of Italy.

Voluntary or Mandated:

Voluntary: Firm initiated