AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water bottle is affected by this recall.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Product Code: 400340, Lot numbers: 001147, 061137, 313147, 059137, 010147, 293137, 038147, 225137, 558137, 362137, 202147, 425137, 301147, 263137, 366137, 076147, 316137, 424137, 012147, 155137, 147137, 597137, 478137, 235147, 278147, 228147, 013147, 303137, 523137, 023147, 206147, 336137, 279147, 481137, 618137, 179137, 025147, 248137, 086147, 252147, 392137, 533137, 551137, 191137, 563137, 270137, 042147, 502137, 080137, 299147, 207137, 022147, 516137, 165137, 387137, 104147, 645137, 220137, 494137, 578137, 385137, 305147, 183137, 390137, 650137, 383137, 041147, 186137, 299137, 246137, 389137, 531137, 027147, 006147, 266137, 236137, 297147, 116147, 189137, 491137, 008147, 208137, 191147, 057137, 480137, 229137, 309137, 611137, 107137, 313137, 163137, 568137, 420137, 474137, 231147, 281147, 234137, 100147, 216137, 300137, 472137, 328137, 485137, 159137, 203147, 353137, 590137, 082147, 556137, 614137, 161137, 469137, 488137, 035147, 194147, 223137, 641137, 489137, 475137, 197147, 024147, 044147, 200147, 203137, 509137, 477137, 213137, 205147, 030147, 594137, 349137, 580137, 190147, 416137, 256147, 033147, 262147, 471137, 413137, 338137, 103137, 149137, 410137, 297137, 346137, 426137, 200137, 569137, 287137, 463137, 575137, 102147, 470137, 582137, 286137, 032147, 307137, 193147, 104137, 290137, 101147, 467137, 572137, 261137, 036147, 197137, 282147, 647137, 103147, 527137, 554137, 331137, 512137, 259137, 505137, 560137, 047147, 125147, 156137, 128147, 305137, 343137, 196147, 465137, 476137, 284147, 391137, 189147, 524137, 078147, 039147, 483137, 334137, 145137, 479137, 549137, 365137, 072147, 253147, 026147, 545137, 283147, 132147, 153137, 407137, 151137, 243137, 136147, 029147, 186147, 227137, 518137, 122147, 356137, 259147, 114147, 194137 & 182137.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Teleflex Medical
- Reason for Recall:
- The packages may contain foreign material (black particles).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water bottle is affected by this recall.
Product Codes/Lot Numbers:
Product Code: 400340, Lot numbers: 001147, 061137, 313147, 059137, 010147, 293137, 038147, 225137, 558137, 362137, 202147, 425137, 301147, 263137, 366137, 076147, 316137, 424137, 012147, 155137, 147137, 597137, 478137, 235147, 278147, 228147, 013147, 303137, 523137, 023147, 206147, 336137, 279147, 481137, 618137, 179137, 025147, 248137, 086147, 252147, 392137, 533137, 551137, 191137, 563137, 270137, 042147, 502137, 080137, 299147, 207137, 022147, 516137, 165137, 387137, 104147, 645137, 220137, 494137, 578137, 385137, 305147, 183137, 390137, 650137, 383137, 041147, 186137, 299137, 246137, 389137, 531137, 027147, 006147, 266137, 236137, 297147, 116147, 189137, 491137, 008147, 208137, 191147, 057137, 480137, 229137, 309137, 611137, 107137, 313137, 163137, 568137, 420137, 474137, 231147, 281147, 234137, 100147, 216137, 300137, 472137, 328137, 485137, 159137, 203147, 353137, 590137, 082147, 556137, 614137, 161137, 469137, 488137, 035147, 194147, 223137, 641137, 489137, 475137, 197147, 024147, 044147, 200147, 203137, 509137, 477137, 213137, 205147, 030147, 594137, 349137, 580137, 190147, 416137, 256147, 033147, 262147, 471137, 413137, 338137, 103137, 149137, 410137, 297137, 346137, 426137, 200137, 569137, 287137, 463137, 575137, 102147, 470137, 582137, 286137, 032147, 307137, 193147, 104137, 290137, 101147, 467137, 572137, 261137, 036147, 197137, 282147, 647137, 103147, 527137, 554137, 331137, 512137, 259137, 505137, 560137, 047147, 125147, 156137, 128147, 305137, 343137, 196147, 465137, 476137, 284147, 391137, 189147, 524137, 078147, 039147, 483137, 334137, 145137, 479137, 549137, 365137, 072147, 253147, 026147, 545137, 283147, 132147, 153137, 407137, 151137, 243137, 136147, 029147, 186147, 227137, 518137, 122147, 356137, 259147, 114147, 194137 & 182137.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1108-2015
Related Recalls
Reports received of torn corrugated breathing tubes.
Reports received of torn corrugated breathing tubes.
The firm received reports indicating PTD tip separation during use.