Recall Z-0303-2023

ROi CPS LLC · initiated October 20, 2022

Class II Terminated

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

Product

regard CVPART1BUNDLE- MERCYSTANTHONY , CV01005H, Item Number 830099008; cardiac surgery convenience kit

Codes / lots: UDI/DI 10194717114895, Lot Numbers: 92534, exp 11/13/2022; 93366, exp 2/28/2023

Reason for recall

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

FDA-determined cause: Component change control

Action taken

ROi CPS, LLC issued a MEDICAL DEVICE CORRECTION NOTICE on 10/20/2022 by email to its consignees. The notice explained the issue, the distribution dates, and kits specific to each consignee, and requested the following: "Actions to be taken by customers: 1. CHECK: Please review your inventory to determine if the manufacturer item numbers and lot numbers listed in the chart above are in your inventory. 2. QUARANTINE: Segregate and quarantine all affected kits in your inventory. 3. LABEL: Use the attached label template (Ro; CPS Correction INC13225-3M Recall Label Template-Avery 5960) to print warning labels to be affixed to all affected kits in your inventory. The label should be applied to each affected Kit and outer product case in a prominently visible location to end-users of the kits. The location chosen should not cover any other critical product information found on the existing product labeling. The label instructs users to remove and discard the 3M Steri-Drapes when the kit is opened for use. 4. REPLY: Complete the reply form included with this notice to indicate your actions in response to this notice. a. If you do not have inventory, please return the form indicating "0" affected inventory at your facility. b. Return the reply form to lacy.stewart@roiscs.com 5. NOTIFY: Please immediately notify any customers to whom you have distributed or forwarded product affected by this medical device correction notice. You may include a copy of this notice, the notice from 3M, and the attached label template with your customer notification. 6. REPORT: Report any adverse health consequences experienced with the 3M products to the FDA's MedWatch Adverse Event Reporting program via: Web: MedWatch website at www.fda.gov/medwatch Phone: 1-800-FDA-1088 (1-800-332-1088) Mail: MedWatch, HF-2, FDA, 5600 Fisher's Lane, Rockville, MD 20852-9787"

Details

Recall number
Z-0303-2023
Initiated
October 20, 2022
Posted by FDA
November 23, 2022
Terminated
April 1, 2026
Product code
OEZ – Cardiovascular Procedure Kit
Quantity
108 kits
Distribution
LA, MO, NC, FL
Recalling firm
ROi CPS LLC, Republic, MO

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0283-2023 Class IIregard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0284-2023 Class IIregard FOOT PACK, OR00123Y, Item Number 880118; orthopedic surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0285-2023 Class IIregard TOTAL JOINT, OR00446F, Item Number 880291; orthopedic surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0286-2023 Class IIregard KYPHOPLASTY, OR01101, Item Number 880469; orthopedic surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0287-2023 Class IIregard BASIC NEURO, NU00259R, Item Number 800021018; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0288-2023 Class IIregard BASIC NEURO, NU00259S, Item Number 800021019; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0289-2023 Class IIregard SPINE PACK, NU00260H, Item Number 800022008; ortho surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0290-2023 Class IIregard VITRECTOMY PACK, EY00266H, Item Number 800028008; eye surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0291-2023 Class IIregard NEURO PACK, NU00278L, Item Number 800040012; nuero surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0292-2023 Class IIregard CERVICAL PACK, NU00303H, Item Number 800058008; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0293-2023 Class IIregard MAJOR EAR, ET00326J, Item Number 800070010; ear surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0294-2023 Class IIregard SHOULDER W BCH CHAIR, OR00356F, Item Number 800203006; ortho surgery convenience…Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0295-2023 Class IIregard SPINE PACK,NU00395J, Item Number 800241010; ortho surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0296-2023 Class IIregard HAND PACK, OR00594K, Item Number 800243011; ortho surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0297-2023 Class IIregard ACDF, NU00698H, Item Number 800246008; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0298-2023 Class IIregard ACDF, NU00698I, Item Number 800246009; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0299-2023 Class IIregard MAJOR CRANI, NU00921E, Item Number 800716005; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0300-2023 Class IIregard RETINAL PACK, EY00935C, Item Number 800730003; EYE surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0301-2023 Class IIregard VITRECTOMY PK, EY00938C, Item Number 800733003; EYE surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0302-2023 Class IIregard SPINE , NU00974F, Item Number 800769006; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0304-2023 Class IIregard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery…Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0305-2023 Class IIregard SHOULDER ARTHROSCOPY, OR00049Q, Item Number 880044017; ortho surgery convenience…Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0306-2023 Class IIregard EYE TRAY, EY00099AE, Item Number 880099031; eye surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0307-2023 Class IIregard FOOT PACK - MERCY SPRINGFIELD , OR00123Z, Item Number 880118026; ortho surgery…Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0308-2023 Class IIregard SHOULDER PK, GS00125U, Item Number 880120021; ortho surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0309-2023 Class IIregard SHOULDER PACK, GS00125V, Item Number 880120022; ortho surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0310-2023 Class IIregard DAVINCI PACK, GS00137W, Item Number 880132023; gastric surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0311-2023 Class IIregard MINOR NEURO, NU00140AD, Item Number 880135030; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0312-2023 Class IIregard NEURO TRAY, NU00160R, Item Number 880158018; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated
Z-0313-2023 Class IIregard SPINE PACK , NU00193N, Item Number 880179014; neuro surgery convenience kitSurgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled. 10/20/2022Terminated