FDA device enforcement
LAP CHOLE 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.
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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 LAP CHOLE PACK. Medical convenience kit.
FDA device enforcement
LAPAROSCOPIC GYN. 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
LAPAROSCOPIC PROSTATECTOMY. 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
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
LAVH 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
MAJOR THORACOSCOPY BASIN. 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
PACK GENERAL ROBOTIC. 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
PARTIAL NEPHRECTOMY - ROBOTIC. 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
PARTIAL NEPHRECTOMY 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
ROBOTIC PROSTATECTOMY 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
ROBOTIC URO/GYN 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
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.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of IL & LA.
FDA device enforcement
Halyard SUTURE PACK CABG. Cardiovascular Procedure 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.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of IL & LA.
FDA device enforcement
Halyard RAPIDES E-PACK. Cardiovascular Procedure 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.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of IL & LA.
FDA device enforcement
Halyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
FDA device enforcement
Halyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
FDA device enforcement
Halyard D & C PACK-CKC - Medical convenience kits Model Number: BMGT003-02
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
FDA device enforcement
Halyard ENT T AND A PACK - Medical convenience kits Model Number: EAMC106-02
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
FDA device enforcement
Halyard OPEN HEART PACK MAIN - Medical convenience kits Model Number: ESJH003-02
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
FDA device enforcement
Halyard AORTA PACK - Medical convenience kits Model Number: ESJH004-02
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 possible foreign body reactions
Class IIReported ongoing
Distribution: US Nationwide distribution.
Reasons in these listed records
- CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 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.
- 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 possible foreign body reactions
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.