smiths medical portex BLUgriggs Percutaneous Dilation Procedural Trays with BLUselect tracheotomy tubes, labeled as f... — FDA record Z-3087-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
smiths medical portex BLUgriggs Percutaneous Dilation Procedural Trays with BLUselect tracheotomy tubes, labeled as follows: 1) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 8.0mm BLUselect trach tube (drugs, US ONLY), Item Number 101/540/080; 2) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 9.0mm BLUselect trach tube (drugs, US ONLY), Item Number 101/540/090; 3) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 7.0mm BLUselect trach tube, Item Number 101/541/070; 4) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 8.0mm BLUselect trach tube, Item Number 101/541/080; 5) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 9.0mm BLUselect trach tube, Item Number 101/541/090; 6) BLUgriggs Percutaneous Dilation Procedural Kit with 7.0mm BLUselect trach tube, no forceps, Item Number 101/543/070; 7) BLUgriggs Percutaneous Dilation Procedural Kit with 8.0mm BLUselect trach tube, no forceps, Item Number 101/543/080; 8) BLUgriggs Percutaneous Dilation Procedural Kit with 9.0mm BLUselect trach tube, no forceps, Item Number 101/543/090; 9) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 7.0mm BLUselect SuctionAid trach tube, Item Number 101/891/070; 10) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 8.0mm BLUselect SuctionAid trach tube, Item Number 101/891/080; 11) BLUgriggs Percutaneous Dilation Procedural Kit with forceps and 9.0mm BLUselect SuctionAid trach tube, Item Number 101/891/090; 12) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 7.0mm BLUselect SuctionAid trach tube (drugs, US ONLY), Item Number 101/892/070; 13) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 8.0mm BLUselect SuctionAid trach tube (drugs, US ONLY), Item Number 101/892/080; 14) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 9.0mm BLUselect SuctionAid trach tube (drugs, US ONLY), Item Number 101/892/090; 15) BLUgriggs Percutaneous Dilation Procedural Kit with 7.0mm BLUselect SuctionAid trach tube, no forceps, Item Number 101/893/070; 16) BLUgriggs Percutaneous Dilation Procedural Kit with 8.0mm BLUselect SuctionAid trach tube, no forceps, Item Number 101/893/080; 17) BLUgriggs Percutaneous Dilation Procedural Kit with 9.0mm BLUselect SuctionAid trach tube, no forceps, Item Number 101/893/090
Reason
There is the potential for a disconnection of the pilot balloon from the tracheostomy inflation line within specific lots of the BLUSelect, BLUgriggs and BLUperc products due to a manufacturing defect.
Classification
Class I
Recalling firm
Smiths Medical ASD Inc.
Quantity
12234 units
Agency-reported status
Ongoing
Source record identifier
Z-3087-2024

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicability101/540/080, Lot Number 3943992; 101/540/080, Lot Number 4258998; 101/540/090, Lot Number 4309778; 101/541/070, Lot Number 3887542; 101/541/070, Lot Number 3913366; 101/541/070, Lot Number 4202486; 101/541/070, Lot Number 4350937; 101/541/080, Lot Number 3887517; 101/541/080, Lot Number 3910324; 101/541/080, Lot Number 3912758; 101/541/080, Lot Number 4170885; 101/541/080, Lot Number 4184037; 101/541/080, Lot Number 4310310; 101/541/080, Lot Number 4312324; 101/541/080, Lot Number 4332049; 101/541/080, Lot Number 4332050; 101/541/090, Lot Number 3887526; 101/541/090, Lot Number 3925818; 101/541/090, Lot Number 4234865; 101/541/090, Lot Number 4266477; 101/541/090, Lot Number 4310313; 101/543/070, Lot Number 3887541; 101/543/070, Lot Number 4310304; 101/543/080, Lot Number 3887527; 101/543/080, Lot Number 3910325; 101/543/080, Lot Number 4310447; 101/543/080, Lot Number 4332051; 101/543/080, Lot Number 4332052; 101/543/080, Lot Number 4332053; 101/543/080, Lot Number 4332054; 101/543/080, Lot Number 4382017; 101/543/080, Lot Number 4382018; 101/543/080, Lot Number 4382019; 101/543/080, Lot Number 4382020; 101/543/080, Lot Number 4382021; 101/543/080, Lot Number 4382022; 101/543/080, Lot Number 4382023; 101/543/080, Lot Number 4382024; 101/543/080, Lot Number 4382025; 101/543/090, Lot Number 3887518; 101/543/090, Lot Number 4384983; 101/891/070, Lot Number 3910414; 101/891/070, Lot Number 3925816; 101/891/070, Lot Number 4117953; 101/891/070, Lot Number 4156869; 101/891/070, Lot Number 4205521; 101/891/070, Lot Number 4232678; 101/891/080, Lot Number 3887523; 101/891/080, Lot Number 3896997; 101/891/080, Lot Number 3896998; 101/891/080, Lot Number 4306752; 101/891/080, Lot Number 4388711; 101/891/090, Lot Number 3913655; 101/891/090, Lot Number 3925770; 101/891/090, Lot Number 4005342; 101/891/090, Lot Number 4310412; 101/892/070, Lot Number 3950087; 101/892/080, Lot Number 3943993; 101/892/080, Lot Number 4165114; 101/892/080, Lot Number 4226926; 101/892/090, Lot Number 3944020; 101/892/090, Lot Number 4194294; 101/893/070, Lot Number 3925807; 101/893/070, Lot Number 4005284; 101/893/070, Lot Number 4005285; 101/893/070, Lot Number 4089723; 101/893/070, Lot Number 4117954; 101/893/070, Lot Number 4138223; 101/893/070, Lot Number 4189353; 101/893/070, Lot Number 4270948; 101/893/070, Lot Number 4281033; 101/893/080, Lot Number 3910326; 101/893/080, Lot Number 3912757; 101/893/080, Lot Number 4005351; 101/893/080, Lot Number 4010052; 101/893/080, Lot Number 4070524; 101/893/080, Lot Number 4165747; 101/893/080, Lot Number 4205522; 101/893/080, Lot Number 4238251; 101/893/080, Lot Number 4281154; 101/893/080, Lot Number 4281202; 101/893/080, Lot Number 4285878; 101/893/080, Lot Number 4289001; 101/893/080, Lot Number 4310416; 101/893/080, Lot Number 4310417; 101/893/080, Lot Number 4310418; 101/893/080, Lot Number 4310419; 101/893/080, Lot Number 4343143; 101/893/080, Lot Number 4382056; 101/893/080, Lot Number 4382057; 101/893/080, Lot Number 4382058; 101/893/080, Lot Number 4382059; 101/893/080, Lot Number 4382060; 101/893/080, Lot Number 4382061; 101/893/090, Lot Number 3925810; 101/893/090, Lot Number 4177907; 101/893/090, Lot Number 4310430; 101/893/090, Lot Number 4310431; 101/893/090, Lot Number 4310432; 101/893/090, Lot Number 4310433; 101/893/090, Lot Number 4310434; 101/893/090, Lot Number 4310435

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Report date
Sep 18, 2024
Recall initiation date
Jun 7, 2024
Center classification date
Sep 11, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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