The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
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Surgical Instruments
🏥 Medical Devices • 6,839 recalls
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
Unintentional shifting of the tip insulation of the firm's electrosurgical probes.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
Class I - Dangerous
Bent transfer catheter tips may cause difficulty or inability in inserting the transfer catheter into the guiding catheter. Potential adverse events that may occur if an affected product is used include increased procedural time, the need for a repeat embryo transfer procedure, or the need for a patient to undergo an additional IVF cycle.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
Angiodynamics Inc. (Navilyst Medical Inc.)
Class I - Dangerous
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.
Class I - Dangerous
The glass syringe used with Pressure Control Syringes may potentially break during use.
Class I - Dangerous
Modified outside of approved manufacturing process
ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
Smiths Medical ASD
Class I - Dangerous
Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may exhibit damage on the safety mechanism guard.
Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
BD has decided to initiate a voluntary recall due to a confirmed complaint trend for droplets of fluid separating from the sealed surface of the MaxZero connector, following disconnection.
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
Valeritas, Incorporated
Class I - Dangerous
There is a potential for "No Needle Demo Units" to contain a needle.
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Centurion Medical Products
Class I - Dangerous
Supplier initiated recall of the GRIPPER Needles
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Becton Dickinson & Company
Class I - Dangerous
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.