Avid Medical Recalls Knee Arthroscopy Kits Due to Foreign Material
Avid Medical is recalling 24 knee arthroscopy kits because they may contain needles with loose polypropylene foreign material.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or hospitalizations, fitting the criteria for a moderate severity score.
Plain-English summary
Avid Medical, Inc. is recalling 24 AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits (Item Code: MADN011-02). The recall is due to the presence of BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
The affected kits were distributed in 10 states: Illinois, Kentucky, Louisiana, Massachusetts, Missouri, New York, Ohio, Texas, Virginia, and Wisconsin. The specific lots involved are 1197468 and 1197469, both with an expiration date of August 1, 2019.
Consumers and healthcare providers should stop using these kits and contact Avid Medical, Inc. for further instructions or a refund.
The recalled product
- Product
- AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02
- Manufacturer
- Avid Medical, Inc.
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 24
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot
- Expiration Date: 1197468
- 8/1/2019
- 1197469
Distribution
Part of a larger recall action
This product is one of 23 recalled by Avid Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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