AVID Medical, Inc. recalls Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Read the official notice →- Date
- 2025-05-21
- Country
- United States
- Brand
- AVID Medical
- Product
- Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
- Classification
- Class II
- Units
- US Nationwide distribution in the states of IL & LA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More AVID Medical recalls
- 2026-02-18
US
AVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Tyvek bag seal issue which may compromise sterility of the kit.
FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of New Jersey.Official notice →- 2026-01-14
US
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Devices are not suitable for organ transplant.
FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of FL, GA and Puerto Rico.Official notice →- 2025-12-24
US
AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Potential for incomplete seal on header bag.
- 2025-09-17
US
AVID Medical, Inc. recalls Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Potential for open header bag seals, compromising sterility.
- 2025-08-13
US
AVID Medical, Inc. recalls GYN ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2024-11-20
US
AVID Medical, Inc. recalls Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or…
Other drugs & medical recalls in the United States
- 2025-05-21
US
Abbott Molecular, Inc. recalls Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR)…
There were reports of an increase in reactive negative controls and false positive results.
US
Foundation Medicine, Inc. recalls FoundationOne Companion Diagnostic (F1CDx)
Four (4) total reports were sent to customers with clinically relevant variants requiring amendment, one (1) of which with an incorrect negative CDx claim. The remaining three (3) with tumor profiling result changes…
FDA · DeviceFoundation Medicine, Inc.Worldwide - US Nationwide distribution in the states of GA, NY and the country…Official notice →US
Meddev Corp recalls Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight,…
Due to mislabeling of products
FDA · DeviceMeddev CorpU.S. Nationwide distribution in the states of CA, CO, CT, FL, IA, IL, MA, ME,…Official notice →US
Nipro Renal Soultions USA, Corporation recalls MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in…
Potential for the presence of visible foreign matter.
FDA · DeviceNipro Renal Soultions USA, CorporationUS Nationwide distribution in the states of AZ, CA, CO, DE, FL, GA, IL, KS,…Official notice →US
Medical Depot Inc. recalls iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a…
Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
FDA · DeviceMedical Depot Inc.Worldwide distribution - US Nationwide and the countries of Albania, Austria,…Official notice →US
Baxter Healthcare Corporation recalls Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.
A cybersecurity vulnerability was discovered through internal testing.