Shent USA, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2229-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: single use accessory devices used through the working channel of a GI endoscope

Product Classification:

Class II

Date Initiated: January 12, 2021

Date Posted: August 18, 2021

Recall Number: Z-2229-2021

Event ID: 88136

Reason for Recall:

Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 230 cm) may actually be catalog #7226 (Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 8 mm x 230 cm) and Devices labeled as catalog #7226, (Grasper/Retriever, Alligator Jaw, Rat Tooth, 2.4 mm x 8 mm x 230 cm) may actually be catalog #7208, Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 230 cm).

Status: Completed

Product Quantity: 47 units (20 US; 27 OUS)

Code Information:

Lot Code: 020377208

Distribution Pattern:

US Nationwide Distribution - CA, CO, MI Foreign: Australia

Voluntary or Mandated:

Voluntary: Firm initiated