Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsator Plus Arterial Blood Gas Sampling Kit (2018-06-26)
In plain language
This recall involves Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsator Plus Arterial Blood Gas Sampling Kits sold in Canada. They are being recalled because the PVP-I Prep Pads included in the kits do not meet the specified povidone iodine concentration over time. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Smiths Medical for specific lot or serial numbers.
- Follow the manufacturer's instructions for return or disposal.
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Affected products
Pro-Vent Plus Arterial Blood Gas Sampling
Model: 4589P-1, 4591P-1, 4599P-1, 4640P-1, 4660P-1, 4699P-1, G1671
Lot: More than 1000 numbers, contact manufacturer.
Anaerobic Pulsator Plus Arterial Blood Sampling
Model: 4057NP-1, 4067NP-1
Lot: More than 100 numbers, contact manufacturer.
Pulsator Liquid Heparin Arterial Blood Sampling Kits
Model: 4039-1
Lot: More than 100 numbers, contact manufacturer.
Dry Pulsator Plus Arterial Blood Sampling Kit
Model: 4044P-1, 4084P-1
Lot: More than 100 numbers, contact manufacturer.
Why this matters
Product defect
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: More than 100 numbers, contact manufacturer., More than 1000 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 4039-1, 4044P-1, 4057NP-1, 4067NP-1, 4084P-1, 4589P-1, 4591P-1, 4599P-1, 4640P-1, 4660P-1, 4699P-1, G1671
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?
Product defect
What should consumers do?
Stop using the product immediately. Contact Smiths Medical for specific lot or serial numbers. Follow the manufacturer's instructions for return or disposal.
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. Product defect
When was this product recalled?
This product was recalled on July 19, 2018.
Is the Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, Dry Pulsator Plus brand affected by this recall?
Yes, Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, Dry Pulsator Plus products are affected by this recall. This recall involves Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsator Plus Arterial Blood Gas Sampling Kits sold in Canada. They are being recalled because the PVP-I Prep Pads included in the kits do not meet the specified povidone iodine concentration over time. Stop using the product and follow the return steps in the official notice.