MHC Medical Products recalls EasyTouch 29G 1ml insulin syringes with incorrect lot numbers on shelf cartons. This may cause confusion in tracking insulin batches.
The retail shelf cartons may be labeled with an incorrect lot number.
MHC Medical Products is recalling EasyTouch 29G 1ml insulin syringes (Item 829155) because shelf cartons may have incorrect lot numbers. This could lead to confusion about which insulin batch is being used, potentially affecting treatment safety.
The shelf cartons may have an incorrect lot number, which could cause confusion about which insulin batch is being used. This might lead to using the wrong insulin batch, potentially affecting treatment safety. However, the hazard does not involve immediate physical harm or malfunction.
People who own or use EasyTouch 29G 1ml insulin syringes (Item 829155) with incorrect lot numbers on the shelf carton. Those most at risk are individuals who rely on precise insulin batch tracking for safe diabetes management.
Check if your EasyTouch 29G 1ml insulin syringe (Item 829155) has a shelf carton labeled with lot number 45014. The product is intended for injection of U100 insulin only.
Verify the lot number on the shelf carton; if it shows 45014, this syringe is part of the recall.
The shelf cartons may have an incorrect lot number, which could cause confusion about which insulin batch is being used.
No, the recall does not require stopping use. The hazard is low risk and only affects lot number labeling.
Check if your EasyTouch 29G 1ml insulin syringe (Item 829155) has a shelf carton labeled with lot number 45014.
We’ve drafted a message you can send MHC Medical Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1779-2018 — MHC Medical Products MHC Medical Products Hello, I own a MHC Medical Products that is covered by recall Z-1779-2018 from MHC Medical Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
