AVID Medical, Inc. recalls

121 recalls on record · latest: March 13, 2026

Official U.S. recall history for AVID Medical, Inc., compiled from official government records.

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AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

March 13, 2026 · Medical device recalls High risk Potential risk for Medline syringe rotating adaptor unwinding during use, which…

AVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

January 2, 2026 · Medical device recalls Moderate risk Tyvek bag seal issue which may compromise sterility of the kit.

AVID Medical, Inc. recalls Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

November 14, 2025 · Medical device recalls Moderate risk Potential for incomplete seal on header bag.

AVID Medical, Inc. recalls Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.

November 14, 2025 · Medical device recalls Moderate risk Potential for incomplete seal on header bag.

AVID Medical, Inc. recalls Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

November 14, 2025 · Medical device recalls Moderate risk Potential for incomplete seal on header bag.

AVID Medical, Inc. recalls Halyard, EP LAB PK. Catalog Number: ESJH009-03.

November 14, 2025 · Medical device recalls Moderate risk Potential for incomplete seal on header bag.

AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.

November 14, 2025 · Medical device recalls Moderate risk Potential for incomplete seal on header bag.

AVID Medical, Inc. recalls Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

November 11, 2025 · Medical device recalls High risk Devices are not suitable for organ transplant.

AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

November 11, 2025 · Medical device recalls High risk Devices are not suitable for organ transplant.

AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

November 11, 2025 · Medical device recalls High risk Devices are not suitable for organ transplant.

AVID Medical, Inc. recalls Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.

August 4, 2025 · Medical device recalls Moderate risk Potential for open header bag seals, compromising sterility.

AVID Medical, Inc. recalls Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.

August 4, 2025 · Medical device recalls Moderate risk Potential for open header bag seals, compromising sterility.

AVID Medical, Inc. recalls DA VINCI PACK URO/PROSTATE. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls CT DAVINCI. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GS ENDOSCOPY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls DAVINCI UROLOGY. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls CARDIAC ROBOT PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GENERAL ROBOTIC PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls HVI CARDIAC ROBOT PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls PARTIAL NEPHRECTOMY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls MAJOR THORACOSCOPY BASIN. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAPAROSCOPY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GEN LAPAROSCOPY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GENERAL LAPAROSCOPY TRAY. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GYN LAPAROSCOPY PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls ROBOTIC URO/GYN PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAPAROSCOPIC TRAY. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAPAROSCOPIC GYN. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAVH PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls PACK GENERAL ROBOTIC. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls LAP CHOLE PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls GYN ROBOTIC PACK. Medical convenience kit.

June 11, 2025 · Medical device recalls Moderate risk CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing d…

AVID Medical, Inc. recalls Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.

March 31, 2025 · Medical device recalls Moderate risk An issue with a raw material used to coat some surgical needles that may result…

AVID Medical, Inc. recalls Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

March 31, 2025 · Medical device recalls Moderate risk An issue with a raw material used to coat some surgical needles that may result…

AVID Medical, Inc. recalls Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

March 31, 2025 · Medical device recalls Moderate risk An issue with a raw material used to coat some surgical needles that may result…