Resource Optimization & Innovation LLC: Medical Device Recall in 2022 - (Recall #: Z-0950-2022)

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:

Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site

Product Classification:

Class II

Date Initiated: February 28, 2022

Date Posted: April 27, 2022

Recall Number: Z-0950-2022

Event ID: 89793

Reason for Recall:

A kit component, the PDI Prevantics Swab, was recalled.

Status: Terminated

Product Quantity: 3,570 kits

Code Information:

a. Manufacturer Item 303403REG; UDI: 20326053105252 Batch/Lot Number 272394, 272723, 273243, 274119, 274222, 275120, 275700, 276890, 277198, 277650, 278195, 278702, 278984, 279240, 279592, 281107, 282148, 282546, 283355, 283758, 283985, 284757, 285260, 286471, 287025, 287757, 287995, 288331, 288535, 289809, 290876, 291283, 292384 b. Manufacturer Item 303404REG; UDI: 20326053105269 Batch/Lot Number 272920, 273244, 273589, 273982, 275005, 275462, 276185, 276898, 277665, 279246, 279597, 283768, 284492, 285144, 285594, 286503, 287537, 288105, 281116, 281378, 281951, 282860, 288553, 288990, 289829, 290601 c. Manufacturer Item 57931 Batch/Lot Number 273102, 275515, 276078, 276342, 277476, 279353, 281577, 282456, 283231, 283246, 284704, 289997, 288248

Distribution Pattern:

US distribution to two consignees located in Missouri

Voluntary or Mandated:

Voluntary: Firm initiated