Bard Medical recalls ArcticGel pads with potential insufficient adhesion to skin. Affected lots include specific catalog numbers and model kits. Consumers should check their product details to determine if they are affected.
Specific lots of ArcticGel Pads have potential issues which may result in the insufficient adhesion of the hydrogel to the pad.
Bard Medical is recalling ArcticGel pads that may not stick properly to the skin during use. This could lead to ineffective temperature management for patients. Affected products include specific pad kits and catalog numbers listed in the recall notice.
The pads may not adhere properly to the skin, which could cause the temperature management system to fail. This might result in improper temperature control for patients during treatment.
Patients using the Arctic Sun temperature management system with these specific ArcticGel pads. Healthcare providers and caregivers who apply the pads to patients are most at risk.
Check the product label for the catalog number and lot number. Affected items include specific pad kits like Intrepid ArcticGel Small Pad Kit (31705I) with lot numbers such as NGAXY602.
Look for the catalog number and lot number on the pad kit to see if it matches the affected items listed in the recall.
Affected pads include Intrepid ArcticGel Small Pad Kit (31705I), Medium Pad Kit (31707I), Large Pad Kit (31709I), and Universal Pad (31700I) with specific lot numbers like NGAXY602.
Check the product label for the catalog number and lot number. Affected items have specific catalog numbers and lot numbers listed in the recall notice.
No action is needed if your pads do not match the affected catalog numbers and lot numbers listed in the recall.
We’ve drafted a message you can send Bard Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1241-2019 — Bard Medical Bard Medical Hello, I own a Bard Medical that is covered by recall Z-1241-2019 from Bard Medical. 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.
