Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
Summary
The FDA issued a Class II for Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile by ROi CPS LLC. Reason: Products are mislabeled with the incorrect product identification on individual kit labeling..
Details
Source
Device Recall
External ID
Z-0693-2022
Action Date
2022-03-09
Status
Terminated
Category
device
Product Description
Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
Lot/Code Info: Item No. 8800297010; Lot No. 90328; UDI 10194717113164
Quantity Affected: 50 kits
Reason for Recall
Products are mislabeled with the incorrect product identification on individual kit labeling.
Distribution
Missouri
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-13
Company
Republic, 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 130 device recalls issued in the same week, part of 403 device-related FDA actions this month.
ROi CPS LLC has 78 FDA actions in our database, including 78 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 (ROi CPS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ROi CPS LLC have FDA actions?
ROi CPS LLC has 78 FDA actions in our database, including 78 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0693-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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