Tamper Evident Additive Port Cap
Last updated
Summary
Product
Tamper Evident Additive Port Cap
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Tamper Evident Additive Port Cap | 58203 | 21-01 |
| Tamper Evident Additive Port Cap | 58590 | 21-01 |
| Tamper Evident Additive Port Cap | 57325 | 21-01 |
| Tamper Evident Additive Port Cap | 56586 | 21-01 |
Issue
The recall was initiated by IMI following their internal discovery that the corrugated shipper box contains incorrect compatibility information. All other information on the box label is correct, including the device label and IFU. Users are advised to not discard or return the device as it is safe to use, and to verify compatibility using the device label and IFU, not the shipper box.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
International Medical Industries, Inc.
2981 Gateway Drive, Pompano Beach, Florida, United States, 33069
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81213
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