FDA recall record

Fort Defiance Industries P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 recall — FDA Z-0121-2022

The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.

Class IIclassification
Z-0121-2022official record ID
Oct 27, 2021report date

Recall record at a glance

Official recordZ-0121-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmFort Defiance Industries, LLC
Report dateOct 27, 2021
Recall initiation dateAug 19, 2021
Quantity380 devices
LocationLoudon, TN, United States

Official product description

P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641

Why the product was recalled

The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.

Distribution information

Distributed nationwide to PA, MD, TX, NJ, OH, TN, UT, VA and internationally to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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