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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