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TELEFLEX MEDICAL Recalls
236 recalls on record · July 25, 2012 to June 1, 2022 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Teleflex Medical, Research Triangle Park, NC, Braided Polyester Rx Only, Sterile, Distributed by Boston Scientific, Nat
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue appr
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 7, 2014Medical DevicesFDA
Teleflex Medical recalls Dekna-lok, 1 x 17.78 cm, Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture USP, Rx On
Hazard: The product did not meet minimum and/or average minimum Teleflex resorption strength requirements.
May 7, 2014Medical DevicesFDA
Teleflex Medical recalls CAPIO, Monodeck, Violet Monofilament Polydioxanone Suture, 1 x 48 inches (122cm) Absorbable Surgical Suture, Rx Only, Te
Hazard: The product did not meet minimum and/or average minimum Teleflex resorption strength requirements.
April 30, 2014Medical DevicesFDA
Teleflex Medical recalls Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48
Hazard: Product does not meet minimum knot tensile strength requirements.
April 30, 2014Medical DevicesFDA
Teleflex Medical recalls Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a gastrointestinal t
Hazard: Sterility of the product cannot be guaranteed.
April 30, 2014Medical DevicesFDA
Teleflex Medical recalls Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E2
Hazard: The products are being recalled because they did not meet minimum diameter requirements.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm), Catalog No. 410944, 5/10 Weck Vista Univers
Hazard: Complaints of leakage of insufflation gas through the device.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access, Catalog No. 405933. An endoscope and accessories is a devic
Hazard: Complaints of leakage of insufflation gas through the device.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 mm Weck Vista Universal Cannula, Catalog No. 405910RC; 5/10/12 mm Weck Vista Universal Cannula, Catalog No. 405912R
Hazard: Complaints of leakage of insufflation gas through the device.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port, Catalog No. 405910R; 5/10/12 mm Weck Vista Optical Bladel
Hazard: Complaints of leakage of insufflation gas through the device.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls 10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C. An endoscope an
Hazard: Complaints of leakage of insufflation gas through the device.
April 9, 2014Medical DevicesFDA
Teleflex Medical recalls Weck Vista Universal Laparoscopic Port, Size 5/10mm x 100mm, Catalog No. 405910, Weck Vista Universal Laparoscopic Port,
Hazard: Complaints of leakage of insufflation gas through the device.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Sutures, Non-absorbable, Silk, Sterile, Rx only, Product Usage: Natural non-absorbable silk surgical suture is a no
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx only, Product Usage: A smooth or thread
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Sutures, Absorbable, Synthetic, Polyglycolic Acid, Sterile, Rx only, Product Usage: Non-absorbable polypropylene su
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Sutures, Non-absorbable, Synthetic, Polypropylene, Sterile, Rx only, Product Usage: Non-absorbable polypropylene su
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Sutures, Non-absorbable, Synthetic, Polyethylene, Sterile, Rx only, Product Usage: Non-absorbable poly(ethylene ter
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Suture, Non-absorbable, Synthetic, Polyamide, Sterile, Rx only, Product Usage: Non-absorbable polyamide surgical su
Hazard: The products are being recalled because they did not meet minimum needle attachment strength requirements.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length (100mm), Product Usage: An endoscope and acc
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length (70mm), Product Usage: An endoscope and
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm), Product Usage: An endoscope and acces
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm), Product Usage: An endoscope and acces
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length (70mm), Product Usage: An endoscope and ac
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS, Product Usage: An endoscope and accessories is a devic
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12 mm Weck¿ Vista" Universal Cannula, Product Usage: An endoscope and accessories is a device used to provide
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port, Product Usage: An endoscope and accessories i
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls 12mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Weck¿ Vista" Universal Laparoscopic Port, Size 5/10/12mmx125mm, Product Usage: An endoscope and accessories is a
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
April 2, 2014Medical DevicesFDA
Teleflex Medical recalls Weck¿ Vista" Universal Laparoscopic Port, Size 5/10/12mmx100mm, Product Usage: An endoscope and accessories is a
Hazard: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.