Recall Z-1006-2022

ROi CPS LLC · initiated March 18, 2022

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Convenience kits containing regard IV Start Kits: regard Clinical Packaging Solutions, Item Number: 830110002, IV01121B - IV Start Labor Birth.

Codes / lots: Lot numbers 89889, exp. 5/12/2022; 90446, exp. 5/12/2022; and 90641, exp. 5/12/2022.

Reason for recall

A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation of test methods used in its manufacture.

FDA-determined cause: Nonconforming Material/Component

Action taken

The recalling firm sent an email to the consignee on 3/18/2022 which said they have attached an Urgent Device Correction Notice for ROi CPS, LLC Convenience Kits that contain Regard branded IV Start Kits that were manufactured using PDI Prevantics products which were recalled by PDI. Attached to the email were the Urgent Device Correction notice dated 3/18/2022, a label template to be used to label the Regard IV start kits contained in the convenience kits, the original recall letter issued by PDI for their Prevantics products that were recalled, and a reply form. The Urgent Device Correction Notice dated 3/18/2022 explained the reason for the recall and listed the affected kit names and identification. The consignee was to review the inventory to determine if the affected kits were in inventory and to segregate and quarantine the kits noting that only the IV Start kit component within the kit was affected and all other items could be used. The customer was to use the attached label template to print warning labels to be affixed to the Regard IV Start Kits contained within the convenience kits. The label was to be applied to each IV Start Kit in a prominently visible location to end users of the kits and the location of the label should not cover any other critical product information found on the existing product label. The labels said 'URGENT PDI PREVANTICS DRUG RECALL DO NOT USE PREVANTICS SWABSTICK OR MAXI SWABSTICK IN THIS KIT PER THE PDI DRUG RECALL NOTICE DATED 2-4-2022 FORWARDED TO YOUR FACILITY." The consignee was to immediately notify any customers to whom the product was distributed or forwarded and the recall notification from the recalling firm, the notice from PDI, and the label template could be forwarded, as well. A reply form was enclosed for completion to indicate response to the notice. The customer was to respond regarding the number of kits in inventory and that they have read and understood the attached notice, forwarded t

Details

Recall number
Z-1006-2022
Initiated
March 18, 2022
Posted by FDA
April 26, 2022
Terminated
August 2, 2024
Product code
LRS – I.V. Start Kit
Quantity
950 convenience kits
Distribution
US Nationwide distribution in the state of Missouri.
Recalling firm
ROi CPS LLC, Republic, MO

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1004-2022 Class IIConvenience kits containing regard IV Start Kits: (1) regard Clinical Packaging…A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation… 03/18/2022Terminated
Z-1005-2022 Class IIConvenience kits containing regard IV Start Kits: (1) regard Clinical Packaging…A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation… 03/18/2022Terminated