FDAClass IIAugust 7, 2019

Sleeve recall

Sleeve, Product Number Sleeve, Part Numbers RESL, SL 3 L, SL 3 M, SL 3 S, L 3 X, SL 3 XS, UESL Product Usage: Products are designed to protect…

Why was Sleeve recalled?

The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter radiation of varying degrees depending on many different variables (e.g., distance, shielding, position, time, kV, etc.). Long-term exposure to scatter radiation may increase the risk of cancer, infertility, or other health-related conditions.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial Numbers: 444749 418756 418757 408712 388138 388139 407957 339006 419340 391212 381909 381862 391205 414767 419574 419561 419562 419190 419189 391214 443199 418796 350481 407814 407813 443198 443200 443201 443197 391203 381803 379683 419191 419192 419107 383262 383261 387157 387158

Product
Sleeve, Product Number Sleeve, Part Numbers RESL, SL 3 L, SL 3 M, SL 3 S, L 3 X, SL 3 XS, UESL Product Usage: Products are designed to protect…
Recalling firm
Burlington Medical, LLC
Quantity
39
Distribution
US Nationwide distribution. The products were distributed to the following foreign countries: Korea, Thailand.
Recall date
August 7, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls