Recall archive
16 recalls · page 1 of 1
Reported Aug 19, 2026Updated Aug 25, 2026
V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand · Product · Product details — The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental…
FDA (openFDA device enforcement)
Reported Nov 19, 2025
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); CFN: SIGSDL45CTVT;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand · Product · Product details — A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatric and thoracic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Potential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery
FDA (openFDA device enforcement)
Reported May 8, 2024
Sofsilk Braided Silk sutures, Product Number S-2782K. Nonabsorbable, sterile, non-mutagenic surgical suture composed of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — One lot of product was exposed to more than the approved number of Ethylene Oxide (EO) sterilization cycles. This may decrease the tensile strength…
FDA (openFDA device enforcement)
Reported Apr 10, 2024
Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Under certain firing conditions, reloads were found to articulate in an uncontrolled manner potentially causing disruption to the staple line. The…
8 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Use of…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Tri-Staple 2.0 Black Intelligent Reload, Product Number SIG60AXT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Affected lots have the potential for a broken sled vane, which may cause the reload to misfire leading to non-functional staple line closure,…
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM C1 (2) 88861747-11 DERMALON* 6-0 BLU 45CM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
11 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Endo Stitch V-Loc 180 Absorbable Reload, Models VLOCA004L, VLOCA006L, VLOCA008L, VLOCA204L, VLOCA206L, VLOCA208L,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Medtronic has received 210 reports of needles breaking during endoscopic suturing. The potential harm(s) include a delay in treatment/therapy, the…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — The affected staplers have the potential for the staple guide to not be securely attached to the instrument. The issue could cause the component to…
FDA (openFDA device enforcement)
Reported Jan 26, 2022
SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — Prior to use on a patient, the device alarm speaker failed to annunciate on power up and the device falsely detected a sensor cable disconnect and…
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Palindrome RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 19 cm, Item Code 8888541019
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Electrostatic Filter Angled, Item Code 350S19006 - Product Usage: indicated for single use on anesthetized patients and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Signia Small Diameter Curved Tip Intelligent Reload 45 mm Vascular/Thin 8 mm - Long Item Code: SIGSDL45CTVT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand · Product · Product details — Potential for the device safety interlock to fail. The safety interlock prevents an empty single-use reload from being erroneously fired a second…
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
Matched: Brand — The device staples may not properly form upon application preventing adequate hemostasis. Use of a product with this assembly error may result in…
8 more products in this recall
FDA (openFDA device enforcement)
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