Medline Custom Procedure Packs recall in Canada: sterility risk
In plain language
This recall involves Medline Custom Procedure Packs containing non-absorbable sutures sold in Canada. They are being recalled because a manufacturing error may compromise the sterile packaging. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Pacemaker PK SHSC-LF
Model: DYNJ46785C
Lot: 22JBS870
Thoracotomy SJHC-LF
Model: DYNJ900799C
Lot: 22FBV582
Gen Trach,Med,Thyroid SJHC-LF
Model: DYNJ900780D
Lot: 22GBD825
Why this matters
Sterility risk
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 22FBV582, 22GBD825, 22JBS870
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: DYNJ46785C, DYNJ900780D, DYNJ900799C
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Sterility risk
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Sterility risk
When was this product recalled?
This product was recalled on January 11, 2023.
Is the Medline Industries, Lp brand affected by this recall?
Yes, Medline Industries, Lp products are affected by this recall. This recall involves Medline Custom Procedure Packs containing non-absorbable sutures sold in Canada. They are being recalled because a manufacturing error may compromise the sterile packaging. Healthcare professionals should contact the manufacturer for more information.