1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
Summary
The FDA issued a Class II for 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack by American Contract Systems, Inc.. Reason: Product was sterilized with a higher than specification EO concentration..
Details
Source
Device Recall
External ID
Z-1037-2022
Action Date
2022-05-18
Status
Ongoing
Category
device
Product Description
1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
Lot/Code Info: 1) ACS Arthroscopy Kit - Model LMAR15R, Lot 981221; UDI: 00191072152978 2) ACS Knee Kit - Model LWKN46N, Lot 966221; UDI: 00191072150158 3) ACS Hand Pack - Model FHHP63T, Lot 966221, UDI: 00191072149954
Quantity Affected: 114 packs
Reason for Recall
Product was sterilized with a higher than specification EO concentration.
Distribution
US Nationwide distribution in the states of IL, MO, NE, and TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-22
Company
Kansas City, MO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 140 device recalls issued in the same week, part of 403 device-related FDA actions this month.
American Contract Systems, Inc. has 188 FDA actions in our database, including 188 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (American Contract Systems, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Contract Systems, Inc. have FDA actions?
American Contract Systems, Inc. has 188 FDA actions in our database, including 188 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1037-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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