Medline Custom Procedure Packs recall in Canada: sterility risk
In plain language
This recall involves Medline Custom Procedure Packs sold in Canada. They are being recalled because a compromised breather pouch may affect the sterility of the medical devices inside. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact Medline Canada Corporation for additional information.
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Affected products
Ensemble Abdo-Perineal
Model: DYNJ38084B
Lot: 23LBR317
Cataract Pack
Model: DYNJ41861
Lot: 23KBB746
Vag Rectal Pack Bh Lf
Model: DYNJ41694B
Lot: 23KBI386
Plastic Limb Sjhc-Lf
Model: DYNJ84997
Lot: 23LBK468
Pacemaker Tegh-Lf
Model: DYNJ46745A
Lot: 23KBB860
Major Gyne Laparoscopy Shsc
Model: DYNJ46774B
Lot: 23LBN531
Pacemaker Set Up Pack
Model: DYNJ40010B
Lot: 23KBA116
Shunt Pack
Model: DYNJ40040C
Lot: 23KBB863
Angiogram Lf
Model: DYNJ41876B
Lot: 23LBM850
Breast Pk Tegh-Lf
Model: DYNJ46717A
Lot: 23LBO013
Eye Trays/Packs
Model: DYNJ41769A
Lot: 23KBB744
Major Cysto Pack
Model: DYNJ41871B
Lot: 23KBN364
Ensemble Pour Accouchement - Lf
Model: DYNJ40933A
Lot: 23LBM102
Oral Surgery Pack Lf
Model: DYNJ41862C
Lot: 23KBF154
Pacemaker Pack Lf
Model: DYNJ41925G
Lot: 24ABA421
Abdominal Hysterectomy Tegh-Lf
Model: DYNJ46730
Lot: 23LBP056
Major Ophthalmic Pack
Model: DYNJ40317
Lot: 24ABC781
Plateau Catheterisme Cardiaque
Model: HCT093J
Lot: 23LBG513
Hernia Appendectomy Tegh-Lf
Model: DYNJ46716
Lot: 23LBM976
Plastic Hand Pack Tegh-Lf
Model: DYNJ46739B
Lot: 24ABG221
Ensemble Surplus Lca- Lf
Model: DYNJ48892C
Lot: 23KBB893
Ensemble Procedure Mineure
Model: DYNJ38085C
Lot: 23LBR333
Vaginal Pack
Model: DYNJ40037A
Lot: 23KBD900
Orl Tympano Pack
Model: DYNJ41674A
Lot: 24ABB568
Cvl Insertion Kit- Lf
Model: CDS984003A
Lot: 23LBO732
Ensemble Main/Poignet
Model: DYNJ59375
Lot: 23LBM752
Ent Pack Cheo-Lf
Model: DYNJ43538B
Lot: 23LBV457
Gen Aurg - Minor-Lf
Model: DYNJ45731A
Lot: 24ABD039
Breast Pack
Model: DYNJ64376
Lot: 24ABD094
Turp Pack Lf
Model: DYNJ41706C
Lot: 24ABG266
Feet, Elbow, And Ankle Tegh-Lf
Model: DYNJ46719B
Lot: 23LBP194
Lft Hrt Cath Radial Access-Lf
Model: DYNJ47667C
Lot: 23LBL629
General Overbed Pack
Model: DYNJ40045B
Lot: 23LBM922
Cysto Pack
Model: DYNJ37171A
Lot: 23LBK417
Apu Line Pack
Model: DYNJ37171A
Lot: 23KBD998
Ep Pack
Model: DYNJ40488
Lot: 23LBL628
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: 23KBA116, 23KBB744, 23KBB746, 23KBB860, 23KBB863, 23KBB893, 23KBD900, 23KBD998, 23KBF154, 23KBI386, 23KBN364, 23LBG513, 23LBK417, 23LBK468, 23LBL628, 23LBL629, 23LBM102, 23LBM752, 23LBM850, 23LBM922, 23LBM976, 23LBN531, 23LBO013, 23LBO732, 23LBP056, 23LBP194, 23LBR317, 23LBR333, 23LBV457, 24ABA421, 24ABB568, 24ABC781, 24ABD039, 24ABD094, 24ABG221, 24ABG266
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: CDS984003A, DYNJ37171A, DYNJ38084B, DYNJ38085C, DYNJ40010B, DYNJ40037A, DYNJ40040C, DYNJ40045B, DYNJ40317, DYNJ40488, DYNJ40933A, DYNJ41674A, DYNJ41694B, DYNJ41706C, DYNJ41769A, DYNJ41861, DYNJ41862C, DYNJ41871B, DYNJ41876B, DYNJ41925G, DYNJ43538B, DYNJ45731A, DYNJ46716, DYNJ46717A, DYNJ46719B, DYNJ46730, DYNJ46739B, DYNJ46745A, DYNJ46774B, DYNJ47667C, DYNJ48892C, DYNJ59375, DYNJ64376, DYNJ84997, HCT093J
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?
Stop using the product immediately. Contact Medline Canada Corporation for 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 October 7, 2024.
Is the Medline Canada Corporation brand affected by this recall?
Yes, Medline Canada Corporation products are affected by this recall. This recall involves Medline Custom Procedure Packs sold in Canada. They are being recalled because a compromised breather pouch may affect the sterility of the medical devices inside. Stop using the product and contact the manufacturer for more information.