ReNovo, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1159-2021)

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:

Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg; PROVISION Reprocessed Smith and Nephew Trocars/ Cannulas (Class I); PROVISION Reprocessed Conmed/ Linvatec Suture Retrievers/ Passers C6387 See updated product list attached for details.

Product Classification:

Class II

Date Initiated: January 19, 2021

Date Posted: March 10, 2021

Recall Number: Z-1159-2021

Event ID: 87258

Reason for Recall:

Non-sterile product was shipped to customers labelled as sterile.

Status: Ongoing

Product Quantity: 81 units

Code Information:

Lot Number L-008926-16037 Lot numbers L-008918-16048, and L-008918-16045 Lot numbers L-008936-16275, and L-008933-16078

Distribution Pattern:

US Nationwide distribution in the states of CA, NJ and OR.

Voluntary or Mandated:

Voluntary: Firm initiated