Reported Jun 1, 2022 · Ongoing
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Teleflex Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: TELEFLEX MEDICAL INC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
5 of 5 products
| # | Product as published |
|---|---|
| 1 | (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile |
| 2 | (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile |
| 3 | (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19061, sterile |
| 4 | (4) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19062, non-sterile |
| 5 | and (5) Gibeck Humid-Vent Filter Compact S with Flex Tube, Product #19812, non-sterile. |
- Lot codes and dates
70 of 70 products
Products covered by this recall # Barcodes Product as published 1 04026704347919(1) Product 17731: KMH21C0130 (01)04026704347919(17)260228(10)KMH21C0130 2 04026704347919KMH21C0162 (01)04026704347919(17)260228(10)KMH21C0162 3 04026704347919KMH21C0262 (01)04026704347919(17)260228(10)KMH21C0262 4 04026704347919KMH21C0265 (01)04026704347919(17)260228(10)KMH21C0265 5 04026704347919KMH21E0077 (01)04026704347919(17)260428(10)KMH21E0077 6 04026704347919KMH21F0231 (01)04026704347919(17)260528(10)KMH21F0231 7 04026704347919KMH21F0276 (01)04026704347919(17)260528(10)KMH21F0276 8 04026704347919KMH21G0428 (01)04026704347919(17)260628(10)KMH21G0428 9 04026704347919KMH21H0142 (01)04026704347919(17)260728(10)KMH21H0142 10 04026704347919KMH21L0020 (01)04026704347919(17)261028(10)KMH21L0020 11 0402670434791904026704347926and KMH22A0068 (01)04026704347919(17)261228(10)KMH22A0068. (2) Product 17732: KMZ21G0733 (01)04026704347926(17)260628(10)KMZ21G0733 12 04026704347926KMZ21G0742 (01)04026704347926(17)260628(10)KMZ21G0742 13 04026704347926KMZ21G0989 (01)04026704347926(17)260628(10)KMZ21G0989 14 04026704347926KMZ21G1049 (01)04026704347926(17)260628(10)KMZ21G1049 15 04026704347926KMZ21K0159 (01)04026704347926(17)260928(10)KMZ21K0159 16 04026704347926KMZ21K0160 (01)04026704347926(17)260928(10)KMZ21K0160 17 04026704347926KMZ21K0275 (01)04026704347926(17)260928(10)KMZ21K0275 18 04026704347926KMZ21K0451 (01)04026704347926(17)260928(10)KMZ21K0451 19 04026704347926KMZ21L0103 (01)04026704347926(17)261028(10)KMZ21L0103 20 04026704347926KMZ21L0602 (01)04026704347926(17)261028(10)KMZ21L0602 - Amount recalled
- 59,581 eaches
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Reports received of torn corrugated breathing tubes.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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