Medical device recalls
Device recalls are the largest single group in this archive, because the FDA logs corrections and removals as well as outright withdrawals. Many are handled entirely between the manufacturer and a hospital and need nothing from a patient. Each notice states who has to act.
13,634 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported Dec 28, 2022
Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tomy International Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Young Dental Manufacturing I, LLC
FDA (openFDA device enforcement)
Reported Dec 21, 2022
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allison Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARROW INTERNATIONAL Inc.
32 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
155 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Oncentra Brachy radiation therapy planning system software.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
PDS II (polydioxanone) Suture- VIOLET MONOFILAMENT 27IN 0 S/A CT-1 Product Code: Z340H For use in soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Leica MICROSYSTEMS Proveo 8, Part Number 10449058, surgical microscope system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)- US. Siemens Material Number (SMN): 10708840…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
STRADIS HEALTHCARE, WECKCELL EYE SPEARS, Item Numbers: a) 9430, b) 9431
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Medical, LLC dba Stradis Healthcare
77 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Dec 21, 2022
NexGen Option Stemmed Tibial Component Size 3, Item Number 00-5986-037-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bunnell, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caire, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
CareFusion V. Mueller CUSHING BAYONET BIPOLAR INSULATED FORCEPS, 0.7MM TIP OVERALL LENGTH 7-1/2" (190MM) , REF F-1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
44 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dewei Medical Equipment Co. Ltd.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Full Vision Inc.
6 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.