Class 2 Device Recall VCare

• Date Initiated by Firm: October 11, 2023
• Date Posted: November 21, 2023
• Recall Status: Open, Classified
• Recall Number: Z-0367-2024
• Recall Event ID: 93237
• 510(K)Number: K012842
• Product Classification: Ventilator, emergency, manual (resuscitator) - Product Code BTM
• Product: Ventlab, LLC V-Care manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. V-Care Child Resuscitator REF #s: VN4100MB, VN4100MCFB-3, VN4100MCP; 2. V-Care Infant Resuscitator REF #s: VN3100OB, VN3100MB-2, VN3100MB-M01, VNW3100MB-2, VN3100MBP-3M, VN3100MB, VN3100MB-D1, VN3100MB-M00-0, VN3100MB-M1, VN3100OBP, VN3100MB-B, VN3100MB-I, VN3100MBP-000, VN3100MBP-2, VN3100MB-PW2, VN3100MBP, VN3100MBP-D1, VN3100MBPW-D2, VN3100MBP-F, VN3100MXK-2, VN3100MX-F, VN3100MC-2, VN3100MC, VN3100MC-B, VN3100MC-D1, VN3100MC-2U, VN3106MC-M1-2V, VN3104MCFB- M01, VN3106MC-D2V, VN3106MC-M1V, VN3100MCP-2, VN3100MCP, VN3106MCPF- M1V, VN3100MBF; 3. V-Care Pediatric Resuscitator REF #s: VN2100MB, VN2102MB, VN2102MBF, VN2102OBP, VN2100MBF, VN2100MBP, VN2100MB-PW, VN2102MX, VN2102MX-F, VN2100MX-M123, VN2100MC, VN2102MC, VN2102MC-B, VN2102MCP, VN2100MCP; 4. V-Care Small Adult Resuscitator REF #s: VN5000MB, VN5002MB, VN5100MB-F, VN5000MBPF, VN5000MBPF-I, VN5000MX, VN5100MX-F, VN5000MX-N, VN5000MXP, VN5000MXP-K, VN5000MC, VN5102MC, VN5100MCP, VN5000MC-N.
• Code Information: ITEM # VN2100MB, UDI-DI: 10889483095379, (Case UDI: 30889483095373); ITEM # VN2100MBF, UDI-DI: 10889483092774, (Case UDI: 30889483092778); ITEM # VN2100MBP, UDI-DI: 10889483108260, (Case UDI: 30889483108264); ITEM # VN2100MB-PW, UDI-DI: 10889483108253, (Case UDI: 30889483108257); ITEM # VN2100MC, UDI-DI: 10889483108277, (Case UDI: 30889483108271); ITEM # VN2100MCP, UDI-DI: 10889483094525, (Case UDI: 30889483094529); ITEM # VN2100MX-M123, UDI-DI: 10889483098936, (Case UDI: 30889483098930); ITEM # VN2102MB, UDI-DI: 10889483105542, (Case UDI: 30889483105546); ITEM # VN2102MBF, UDI-DI: 10889483110966, (Case UDI: 30889483110960); ITEM # VN2102MC, UDI-DI: 10889483111994, (Case UDI: 30889483111998); ITEM # VN2102MC-B, UDI-DI: 10889483107393, (Case UDI: 30889483107397); ITEM # VN2102MCP, UDI-DI: 10889483088470, (Case UDI: 30889483088474); ITEM # VN2102MX, UDI-DI: 10889483095751, (Case UDI: 30889483095755); ITEM # VN2102MX-F, UDI-DI: 10889483105863, (Case UDI: 30889483105867); ITEM # VN2102OBP, UDI-DI: 10889483108895, (Case UDI: 30889483108899); ITEM # VN3100MB, UDI-DI: 10889483096994, (Case UDI: 30889483096998); ITEM # VN3100MB-2, UDI-DI: 10889483105900, (Case UDI: 30889483105904); ITEM # VN3100MB-B, UDI-DI: 10889483113585, (Case UDI: 30889483113589); ITEM # VN3100MB-D1, UDI-DI: 10889483105566, (Case UDI: 30889483105560); ITEM # VN3100MBF, UDI-DI: 10889483100622, (Case UDI: 30889483100626); ITEM # VN3100MB-I, UDI-DI: 10889483109380, (Case UDI: 30889483109384); ITEM # VN3100MB-M00- 0, UDI-DI: 10889483095980, (Case UDI: 30889483095984); ITEM # VN3100MB-M01, UDI-DI: 10889483110386, (Case UDI: 30889483110380); ITEM # VN3100MB-M1, UDI-DI: 10889483102763, (Case UDI: 30889483102767); ITEM # VN3100MBP, UDI-DI: 10889483100622, (Case UDI: 30889483100626); ITEM # VN3100MBP-000, UDI-DI: 10889483110393, (Case UDI: 30889483110397); ITEM # VN3100MBP-2, UDI-DI: 10889483104262, (Case UDI: 30889483104266); ITEM # VN3100MBP-3M, UDI-DI: 10889483100639, (Case UDI: 30889483100633); ITEM # VN3100MBP-D1, UDI-DI: 10889483110751, (Case UDI: 30889483110755); ITEM # VN3100MBP-F, UDI-DI: 10889483102770, (Case UDI: 30889483102774); ITEM # VN3100MB-PW2, UDI-DI: 10889483110744, (Case UDI: 30889483110748); ITEM # VN3100MBPW-D2, UDI-DI: 10889483111192, (Case UDI: 30889483111196); ITEM # VN3100MC, UDI-DI: 10889483100646, (Case UDI: 30889483100640); ITEM # VN3100MC-2, UDI-DI: 10889483111208, (Case UDI: 30889483111202); ITEM # VN3100MC-2U, UDI-DI: 10889483112113, (Case UDI: 30889483112117); ITEM # VN3100MC-B, UDI-DI: 10889483095768, (Case UDI: 30889483095762); ITEM # VN3100MC-D1, UDI-DI: 10889483112021, (Case UDI: 30889483112025); ITEM # VN3100MCP, UDI-DI: 10889483110768, (Case UDI: 30889483110762); ITEM # VN3100MCP-2, UDI-DI: 10889483113622, (Case UDI: 30889483113626); ITEM # VN3100MX-F, UDI-DI: 10889483112038, (Case UDI: 30889483112032); ITEM # VN3100MXK-2, UDI-DI: 10889483111215, (Case UDI: 30889483111219); ITEM # VN3100OB, UDI-DI: 10889483099964, (Case UDI: 30889483099968); ITEM # VN3100OBP, UDI-DI: 10889483105924, (Case UDI: 30889483105928); ITEM # VN3104MCFB- M01, UDI-DI: 10889483110775, (Case UDI: 30889483110779); ITEM # VN3106MC-D2V, UDI-DI: 10889483107539, (Case UDI: 30889483107533); ITEM # VN3106MC-M1- 2V, UDI-DI: 10889483095997, (Case UDI: 30889483095991); ITEM # VN3106MC-M1V, UDI-DI: 10889483097991, (Case UDI: 30889483097995); ITEM # VN3106MCPF- M1V, UDI-DI: 10889483099001, (Case UDI: 30889483099005); ITEM # VN4100MB, UDI-DI: 10889483111338, (Case UDI: 30889483111332); ITEM # VN4100MCFB-3, UDI-DI: 10889483111239, (Case UDI: 30889483111233); ITEM # VN4100MCP, UDI-DI: 10889483098042, (Case UDI: 30889483098046); ITEM # VN5000MB, UDI-DI: 10889483112052, (Case UDI: 30889483112056); ITEM # VN5000MBPF, UDI-DI: 10889483112229, (Case UDI: 30889483112223); ITEM # VN5000MBPF-I, UDI-DI: 10889483113646, (Case UDI: 30889483113640); ITEM # VN5000MC, UDI-DI: 10889483095393, (Case UDI: 30889483095397); ITEM # VN5000MC-N, UDI-DI: 10889483108352, (Case UDI: 30889483108356); ITEM # VN5000MX, UDI-DI: 10889483107782, (Case UDI: 30889483107786); ITEM # VN5000MX-N, UDI-DI: 10889483107553, (Case UDI: 30889483107557); ITEM # VN5000MXP, UDI-DI: 10889483089828, (Case UDI: 30889483089822); ITEM # VN5000MXP-K, UDI-DI: 10889483110409, (Case UDI: 30889483110403); ITEM # VN5002MB, UDI-DI: 10889483100660, (Case UDI: 30889483100664); ITEM # VN5100MB-F, UDI-DI: 10889483107560, (Case UDI: 30889483107564); ITEM # VN5100MCP, UDI-DI: 10889483098554, (Case UDI: 30889483098558); ITEM # VN5100MX-F, UDI-DI: 10889483095782, (Case UDI: 30889483095786); ITEM # VN5102MC, UDI-DI: 10889483109403, (Case UDI: 30889483109407); ITEM # VNW3100MB-2, UDI-DI: 10889483100677, (Case UDI: 30889483100671). All lots manufactured from 9/21/2018 to present. Latest expiration Date 10/11/2028.
• Recalling Firm/ Manufacturer: SunMed Holdings, LLC; 2710 Northridge Dr Nw Ste A; Grand Rapids MI 49544-9112
• For Additional Information Contact: Jessica Hoke; 800-433-2797
• Manufacturer Reason for Recall: A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
• FDA Determined Cause: Device Design
• Action: Customer notification was emailed October 11, 2023 advising customers that monitoring of tidal carbon dioxide in critically ill patients is recommended because use of accessories (e.g. PEEP valve) on the exhalation port of manual resuscitators may increase backward leak in the integrated manometer due to increased expiratory resistance. This affects all lots with duckbill-style patient valve with integrated manometer manufactured since 09/21/2019. Customers are to disseminate this information to all users and complete and return the response for. The notice also notes manual resuscitator IFUs will be updated to include this information as a warning statement.
• Distribution: US Nationwide distribution including in the states of AR, AZ, CA¿CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, NC, ND, NH, NJ, NM, NV, NY, OH, SC, TN, TX, UT, VA, & WV.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.

• 510(K) Database: 510(K)s with Product Code = BTM