FDA device enforcement
Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Iowa.
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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, Towel Six Pack. Kit Code: AMTS70-01.
FDA device enforcement
Halyard, Drape Pack. Kit Code: LMDP36-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Iowa.
FDA device enforcement
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Iowa.
FDA device enforcement
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into...
Class IReported ongoing
Distribution: US Nationwide distribution in the states of NC and TX.
FDA device enforcement
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into...
Class IReported ongoing
Distribution: US Nationwide distribution in the states of NC and TX.
FDA device enforcement
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into...
Class IReported ongoing
Distribution: US Nationwide distribution in the states of NC and TX.
FDA device enforcement
Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard CATH LAB kit. Model Number: SACL75AM.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard CATH LAB kit. Model Number: SACL75-01.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IReported ongoing
Distribution: US distribution to FL, IL, MO, MS, NC, NE, TX.
FDA device enforcement
Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Tyvek bag seal issue which may compromise sterility of the kit.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of New Jersey.
FDA device enforcement
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
Potential for incomplete seal on header bag.
Class IIReported ongoing
Distribution: US distribution to GA, IL, NE, MD.
FDA device enforcement
Halyard, EP LAB PK. Catalog Number: ESJH009-03.
Potential for incomplete seal on header bag.
Class IIReported ongoing
Distribution: US distribution to GA, IL, NE, MD.
FDA device enforcement
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Potential for incomplete seal on header bag.
Class IIReported ongoing
Distribution: US distribution to GA, IL, NE, MD.
Reasons in these listed records
- Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation a...
- Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- Tyvek bag seal issue which may compromise sterility of the kit.
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.