FDA device enforcement
Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.
Potential for incomplete seal on header bag.
Class IIReported ongoing
Distribution: US distribution to GA, IL, NE, MD.
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AVID Medical, Inc. recall records
147 reported ongoing
147 records in this archive. Latest source date Aug 10, 2026.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Records and reported status
Official source for Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.
FDA device enforcement
Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.
Potential for incomplete seal on header bag.
Class IIReported ongoing
Distribution: US distribution to GA, IL, NE, MD.
FDA device enforcement
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
Devices are not suitable for organ transplant.
Class IReported ongoing
Distribution: US Nationwide distribution in the states of FL, GA and Puerto Rico.
FDA device enforcement
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Devices are not suitable for organ transplant.
Class IReported ongoing
Distribution: US Nationwide distribution in the states of FL, GA and Puerto Rico.
FDA device enforcement
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Devices are not suitable for organ transplant.
Class IReported ongoing
Distribution: US Nationwide distribution in the states of FL, GA and Puerto Rico.
FDA device enforcement
Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Potential for open header bag seals, compromising sterility.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Florida.
FDA device enforcement
Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.
Potential for open header bag seals, compromising sterility.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Florida.
FDA device enforcement
LAPAROSCOPIC TRAY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
CARDIAC ROBOT PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
CT DAVINCI. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
DA VINCI PACK URO/PROSTATE. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
DAVINCI UROLOGY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GEN LAPAROSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GENERAL LAPAROSCOPY TRAY. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GENERAL ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GS ENDOSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GYN LAPAROSCOPY PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
GYN ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
FDA device enforcement
HVI CARDIAC ROBOT PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Class IIReported ongoing
Distribution: Domestic: CA, IL, MD, OH, PA, TX, WA.
Reasons in these listed records
- Potential for incomplete seal on header bag.
- Devices are not suitable for organ transplant.
- Potential for open header bag seals, compromising sterility.
- CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
These examples come from this result page and are not a ranking of every recall reason.
Checking AVID Medical, Inc.
Is there a recall on avid medical, inc. right now?
This archive contains 147 records, including 147 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
How do I check my package or product?
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
Does a matching name mean every item is included?
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
What if the search finds no matching record?
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Where can I find older records?
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.