Recall archive
7 recalls · page 1 of 1
Reported Feb 10, 2021
REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergan PLC
Matched: Brand — Missing Instruction For Use insert.
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 Oz bottle, Distributed in the U.S.A. by Allergan, Irvine,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
Matched: Brand · Product · Product details — SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
Matched: Brand — The firm has became aware that 2D barcodes on breast implants and sizers may be unreadable by GS-1 configured scanners. These 2D barcodes contain a…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergan PLC
Matched: Brand · Reason for recall — Residual polishing compounds, that are used in the needle sleeve manufacturing process, may be present on the injector needle. The residual polishing…
FDA (openFDA device enforcement)
Reported Sep 18, 2019
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Allergan PLC
Matched: Brand — The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence…
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2019
Allergan plc recalls BIOCELL® BIOCELL® textured breast implants and tissue expanders due to Due to uncommon incidence of breast implant-associated anaplastic…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Allergan PLC
Matched: Brand · Product — Due to uncommon incidence of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL)
FDA (recalls & safety alerts)
Reported Mar 7, 2018
REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LifeCell Corporation, A Wholly Owned Subsidiary
Matched: Brand — Presence of bacterial endotoxins levels above the acceptable limit
FDA (openFDA device enforcement)
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