3M recalls Model 63700 Bair Hugger temperature blankets due to potential airflow issues causing limited inflation. Affected units have lot number FR10361.
Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming Blanket, Models 63500 and 63700, can make these blankets more susceptible to unintended occlusion of airflow resulting in limited or partial inflation during use.
3M is recalling its Model 63700 Bair Hugger temperature blankets because a design change may cause them to inflate less than intended during use. This could lead to inadequate temperature management for patients.
The design change makes the blanket more prone to blocking airflow, which can limit or partially inflate the blanket during use. This may cause the system to fail in maintaining proper patient temperature.
Healthcare providers using the 3M Bair Hugger Model 63700 for patient temperature management are most at risk. Patients receiving this equipment may experience temperature issues if the blanket doesn't inflate properly.
Check for the Model 63700 label on the blanket. Affected units have lot number FR10361. The product is used for patient temperature management in healthcare settings.
Look for the Model 63700 label on the blanket and lot number FR10361.
The recall indicates a potential risk of limited inflation during use, so users should check if they have the recalled model and follow the action steps.
The recall does not specify a remedy, so check the model and lot number and contact 3M for further instructions.
Affected units have the Model 63700 label and lot number FR10361. Check the product label for these details.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-0599-2018 — 3M 3M Hello, I own a 3M that is covered by recall Z-0599-2018 from 3M. 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.
