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FDAFDA · Food and drugs·Recall number Z-0361-2024

Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to include: 1. AirFlow Adult Resuscitator REF #s: AF1140MB-M5, AF1140MB-D5, AF5142OB, AF5142MB, AF5142MB-D235, AF1142MBP, AF5142MBP, AF5140MB, AF5140MB-2, AF5140MB-D6, AF5140MB-F, AF1140MB-T, AF1140MB-PW, AF5140MB-PW, AF1140MB-I, AF5140MB-I, AF5140MBN, AF1140MBS, AF5140MBS, AF1140MB-X, AF5140MB-X, AF1140MB-P, AF5140MBP, AF1140MB-K, AF5140MBS-I,AF5140MBPF-G10, AF5140MBP-G10, AF1140MBP-T, AF5140MBP-I, AF1140MBP-K, AF1140MBC-N, AF1140MBP-2, AF1140MC, AF5140MC, AF1140MCP, AF5140MC-P, AF1100MB, AF5100MB, AF5100MC, AF1140MC-M5, AF1140MB-TM5, AF1140MBP-TM5, AF1100MC, AF1140OB, AF1140MBP-M5, AFW1140MB,AF1140MBS-P, AF1000MBN-20, AF5102MBP, AF1100MB-N, AF1100MC-P, AF1140MB, AF1140MB-E, AF1140MB-N, AF1140MB-R, AF1140MBS-K, AF1140MBSP-I, AF1142MB, AF1100MBS, AF1100MB-MMC, AF1100MB-PWG1, AF1100MBP; 2. AirFlow Child Resuscitator REF #s: AF4100MCP, AF4140MB, AF4140MB-I, AF4140MBP, AF4140MB-PI, AF4100MB, AF4100MBP, AF4100OB, AF4140MB-D23, AF4140OBP, AF4140MCP-D3, AF4140MC; 3. AirFlow Infant Resuscitator REF #s: AF3140OB, AF3144MB, AF3104MB-PW, AF3100MBP- M0D1, AF3100MBP- M012, AF3140MB-M000, AF3140MB-D2, AF3140MB-D1, AF3140MB-S1, AF3140MB-2B, AF3140MB-I, AF3140MB-K, AF3100MB-PW, AF3100MB-PTS1, AF3100MB-M0- D1, AF3100OC, AF3100MC-2, AF3100MC, AF3106MC-2, AF3140MCP-K, AF3140MC-2B, AF3100MCP-2, AF3140MC- M0D12, AF3144MCP- M1M00, AF3100OB, AF3140MB, AF3140MB-M0, AF3140MB-2, AF3140MB-M1, AF3140MB-PW, AF3140MB-P, AF3140MB-D12I, AF3140MBP-2, AF3140MC, AF3140MCP, AF3140MCPF, AF3100MB, AF3100MB-M0, AF3100MB-2, AF3100MB-M1, AF3100MB-X, AF3100MBP, AF3100MB-M01, AF3100MBP-M01, AF3100MBP-2, AF3100MBP-D12, AF3100MCP; 4. AirFlow Pediatric Resuscitator REF #s: AF2100OB, AF2100MB-3, AF2102OB, AF2100MB-D5, AF2140OB, AF2102MBP-2, AF2102MBPW-D4, AF2102MBP-M3, AF2140MB-2, AFW2142OB, AF2140MB-D4, AF2140MB-D43, AF2140MB-P2, AF2144MB, AFW2142MB-2, AF2142MB-D3, AF2242MBP, AF2142MBS-I, AF2142MBP- 224OT, AF2140MBPW- D23, AF2140MB-I, AF2140MB-K, AF2140MB-S, AF2140MBP-K, AF2100MB-PW, AF2100MB-MMC, AF2102MBP, AF2100MB- PWTS4, AF2140MCPF, AF2100MC, AF2102MC, AF2142MC-M01, AF2140MC, AF2142MC-D34, AF2140MCP-D4, AF2140MC-PT, AF2140MCP-K, AF2142MCP, AF2100MCP, AF2102MB, AF2102MCP, AF2102MC-PT, AF2142OB, AF2142OBNS, AF2142MB, AF2142MB-3, AF2142MB-2, AF2142MB-M5E, AF2142MB-PW, AF2142MBP, AF2142MB-K, AF2142MBP-2, AF2142MC-3, AF2142MCP-D4, AF2140MB, AF2140MB-PW, AF2140MBP, AF1142OB, AF2100MB; 5. AirFlow Small Adult Resuscitator REF #s: AF5140MC-D6, AF5140MB-M5, AF5100MB-D5, AF5142MBP-M5, AF5140MBPW-D5, AF5140MBPWTD5, AF5140MBP-D5, AF5140MBP-D6, AF5140MBPW- M5, AF5140MBP-M5, AFN5140MB, AF5140MB-OT, AF5140MB-T, AFD5140MB-T, AF5140MB-K, AF5140MBS-R, AF5140MBS-P, AF5140MB-PT, AF5140MB-ST, AF5140MCP-K, AF5100MB-PW, AF5102MB-N, AF5140MBS-M5. 6. Ventlab, LLC Resuscitation Kit REF # MC1000.

Published November 29, 2023 · Recall initiated: October 11, 2023

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
SunMed Holdings, LLC
Distributor
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.
Lot
UDI-DI: 10889483075814 (Item # AF1000MBN-20, Case UDI: 30889483075818); UDI-DI: 10889483076606 (Item # AF1100MB, Case UDI: 30889483076600); UDI-DI: 10889483076613 (Item # AF1100MB-MMC, Case UDI: 30889483076617); UDI-DI: 10889483075838 (Item # AF1100MB-N, Case UDI: 30889483075832); UDI-DI: 10889483088074 (Item # AF1100MBP, Case UDI: 30889483088078); UDI-DI: 10889483086209 (Item # AF1100MB-PWG1, Case UDI: 30889483086203); UDI-DI: 10889483086216 (Item # AF1100MBS, Case UDI: 30889483086210); UDI-DI: 10889483094365 (Item # AF1100MC, Case UDI: 30889483094369); UDI-DI: 10889483159217 (Item # AF1100MC-P, Case UDI: 30889483159211); UDI-DI: 10889483071809 (Item # AF1140MB, Case UDI: 30889483071803); UDI-DI: 10889483230626 (Item # AF1140MBC-N Case UDI: 30889483230620); UDI-DI: 10889483090718 (Item # AF1140MB-D5, Case UDI: 30889483090712); UDI-DI: 10889483106372 (Item # AF1140MB-E, Case UDI: 30889483106376); UDI-DI: 10889483095096 (Item # AF1140MB-I, Case UDI: 30889483095090); UDI-DI: 10889483083918 (Item # AF1140MB-K, Case UDI: 30889483083912); UDI-DI: 10889483162224 (Item # AF1140MB-M5, Case UDI: 30889483162228); UDI-DI: 10889483094372 (Item # AF1140MB-N, Case UDI: 30889483094376); UDI-DI: 10889483098370 (Item # AF1140MB-P, Case UDI: 30889483098374); UDI-DI: 10889483101469 (Item # AF1140MBP-2, Case UDI: 30889483101463); UDI-DI: 10889483106396 (Item # AF1140MBP-K, Case UDI: 30889483106390); UDI-DI: 10889483076637 (Item # AF1140MBP-M5, Case UDI: 30889483076631); UDI-DI: 10889483078143 (Item # AF1140MBP-T, Case UDI: 30889483078147); UDI-DI: 10889483162637 (Item # AF1140MBP-TM5, Case UDI: 30889483162631); UDI-DI: 10889483098387 (Item # AF1140MB-PW, Case UDI: 30889483098381); UDI-DI: 10889483074190 (Item # AF1140MB-R, Case UDI: 30889483074194); UDI-DI: 10889483095119 (Item # AF1140MBS, Case UDI: 30889483095113); UDI-DI: 10889483093320 (Item # AF1140MBS-K, Case UDI: 30889483093324); UDI-DI: 10889483076422 (Item # AF1140MBS-P, Case UDI: 30889483076426); UDI-DI: 10889483089088 (Item # AF1140MBSP-I, Case UDI: 30889483089082); UDI-DI: 10889483087213 (Item # AF1140MB-T, Case UDI: 30889483087217); UDI-DI: 10889483162439 (Item # AF1140MB-TM5, Case UDI: 30889483162433); UDI-DI: 10889483227589 (Item # AF1140MB-X, Case UDI: 30889483227583); UDI-DI: 10889483101476 (Item # AF1140MC, Case UDI: 30889483101470); UDI-DI: 10889483163146 (Item # AF1140MC-M5, Case UDI: 30889483163140); UDI-DI: 10889483097359 (Item # AF1140MCP, Case UDI: 30889483097353); UDI-DI: 10889483102121 (Item # AF1140OB, Case UDI: 30889483102125); UDI-DI: 10889483078150 (Item # AF1142MB, Case UDI: 30889483078154); UDI-DI: 10889483089255 (Item # AF1142MBP, Case UDI: 30889483089259); UDI-DI: 10889483089095 (Item # AF1142OB, Case UDI: 30889483089099); UDI-DI: 10889483096390 (Item # AF2100MB, Case UDI: 30889483096394); UDI-DI: 10889483076019 (Item # AF2100MB-3, Case UDI: 30889483076013); UDI-DI: 10889483171578 (Item # AF2100MB-D5, Case UDI: 30889483171572); UDI-DI: 10889483078181 (Item # AF2100MB-MMC, Case UDI: 30889483078185); UDI-DI: 10889483159231 (Item # AF2100MB-PW, Case UDI: 30889483159235); UDI-DI: 10889483102138 (Item # AF2100MB- PWTS4, Case UDI: 30889483102132); UDI-DI: 10889483090749 (Item # AF2100MC, Case UDI: 30889483090743); UDI-DI: 10889483101506 (Item # AF2100MCP, Case UDI: 30889483101500); UDI-DI: 10889483095706 (Item # AF2100OB, Case UDI: 30889483095700); UDI-DI: 10889483098394 (Item # AF2102MB, Case UDI: 30889483098398); UDI-DI: 10889483112977 (Item # AF2102MBP, Case UDI: 30889483112971); UDI-DI: 10889483076644 (Item # AF2102MBP-2, Case UDI: 30889483076648); UDI-DI: 10889483097304 (Item # AF2102MBP-M3, Case UDI: 30889483097308); UDI-DI: 10889483172285 (Item # AF2102MBPW-D4, Case UDI: 30889483172289); UDI-DI: 10889483158883 (Item # AF2102MC, Case UDI: 30889483158887); UDI-DI: 10889483078198 (Item # AF2102MCP, Case UD
Risk classification
Class II
Area (FDA)
device
Country
United States

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