AVID Medical, Inc. recalls
65 recalls filed under AVID Medical, Inc.. The most recent was published May 13, 2026.
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Class I · 6 months ago
AVID Medical, Inc. Halyard CATH LAB kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class I · 6 months ago
AVID Medical, Inc. Halyard Cardiac Cath Pack kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class I · 6 months ago
AVID Medical, Inc. Halyard CATH LAB kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class I · 6 months ago
AVID Medical, Inc. Halyard VA Detroit Cath LAB Pack kit. Model Numbers: Vmcd029 recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class I · 6 months ago
AVID Medical, Inc. Halyard Cardiac Cath Pack SAN23Cardq kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class I · 6 months ago
AVID Medical, Inc. Halyard Cardiac Cath Tray Shands JAX kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
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Class II · 8 months ago
AVID Medical, Inc. Halyard Transport BAG KIT. Kit Code: Life0080-01 recall: Tyvek bag seal issue which may compromise sterility of the kit
Tyvek bag seal issue which may compromise sterility of the kit.
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Class I · 9 months ago
AVID Medical, Inc. Halyard Mini Plus KIT South, Kit Code: Jack097-08 recall: Devices are not suitable for organ transplant
Devices are not suitable for organ transplant.
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Class I · 9 months ago
AVID Medical, Inc. Halyard Organ Recovery OR Pack, Kit Code: Llog1000-15 recall: Devices are not suitable for organ transplant
Devices are not suitable for organ transplant.
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Class I · 9 months ago
AVID Medical, Inc. Halyard Organ Recovery OR Pack, Kit Code: Llof1000-17 recall: Devices are not suitable for organ transplant
Devices are not suitable for organ transplant.
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Class II · 10 months ago
AVID Medical, Inc. Halyard, General Laparoscopy Pack recall: Potential for incomplete seal on header bag
Potential for incomplete seal on header bag.
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Class II · 10 months ago
AVID Medical, Inc. Halyard, Head AND Neck Tray recall: Potential for incomplete seal on header bag
Potential for incomplete seal on header bag.
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Class II · 10 months ago
AVID Medical, Inc. Halyard, Major Pack recall: Potential for incomplete seal on header bag
Potential for incomplete seal on header bag.
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Class II · 10 months ago
AVID Medical, Inc. Halyard, EP LAB PK recall: Potential for incomplete seal on header bag
Potential for incomplete seal on header bag.
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Class II · 10 months ago
AVID Medical, Inc. Halyard, Midtown General Arteriogram recall: Potential for incomplete seal on header bag
Potential for incomplete seal on header bag.
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Class II · 1+ years ago
AVID Medical, Inc. Halyard, CPT Basic IR Pack recall: Potential for open header bag seals, compromising sterility
Potential for open header bag seals, compromising sterility.
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Class II · 1+ years ago
AVID Medical, Inc. Halyard, ENT PACK recall: Potential for open header bag seals, compromising sterility
Potential for open header bag seals, compromising sterility.
About this page
AVID Medical, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.