Recall archive
9 recalls · page 1 of 1
Reported Jul 8, 2026
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand — Due to out-of-specification, or potential out-of-specification, levels of endotoxins
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand — There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex LLC
Matched: Brand — Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
122 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2023
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand · Product · Product details · Reason for recall — Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that…
FDA (openFDA device enforcement)
Reported May 24, 2023
Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand · Product · Product details — The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has…
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand — Potential for pilot balloon non-inflation or cuff non-deflation.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Pilling Wecksorb Cylindrical Sponges
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand — Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
Matched: Brand · Product · Product details — Product may not be sterile
FDA (openFDA device enforcement)
Reported Oct 26, 2022
Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex LLC
Matched: Brand — Incidents of device splitting or detaching during use
5 more products in this recall
FDA (openFDA device enforcement)
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