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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

Burlington Medical Radiation Protection Products Recalled for Shielding Defect

Agency Publication Date: April 2, 2026
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Summary

Burlington Medical, LLC is recalling 96,395 radiation protection garments and accessories, including thyroid shields, vests, kilts, and aprons, because the internal shielding material may degrade over time. This defect can shorten the protective lifespan of the equipment, which is used by healthcare professionals to block radiation during medical procedures. The affected products were manufactured between January 16, 2025, and January 21, 2026, and use Xenolite 800 attenuation material.

Risk

The radiation shielding material may break down faster than expected, reducing the amount of protection provided to the wearer. This increases the risk of accidental radiation exposure to healthcare staff and patients during diagnostic or surgical imaging.

What You Should Do

  1. Identify your garment by checking the product label for the model name (such as Thyroid Shield, Vest, Kilt, or Frontal Apron) and the serial number.
  2. Check if your product was manufactured with Xenolite 800 attenuation material between the dates of January 16, 2025, and January 21, 2026.
  3. Because there are hundreds of affected model numbers and over 96,000 serial numbers, see the Affected Products section below for the full list of affected codes.
  4. Stop using the recalled product. Contact Burlington Medical, LLC or your authorized distributor to arrange for a return, replacement, or correction of the garment.
  5. Call the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for more information.

Your Remedy Options

📋Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Burlington Medical, Thyroid Shield
Variants: Xenolite 800 attenuation material
Model / REF (108):
R8COPEH
R8TSBBB
R8TSBBN
R8TSBBR
R8TSBBT
R8TSBHB
R8TSBHN
R8TSBHR
R8TSBHT
R8TSBMB
R8TSBMN
R8TSBMR
R8TSBMT
R8TSCBB
R8TSCBN
R8TSCBR
R8TSCBS
R8TSCBT
R8TSCHB
R8TSCHN
R8TSCHR
R8TSCHS
R8TSCHT
R8TSCMB
R8TSCMN
R8TSCMR
R8TSCMS
R8TSCMT
R8TSOBB
R8TSOBN
R8TSOBR
R8TSOHB
R8TSOHR
R8TSOHT
R8TSOMN
R8TSOMR
R8TSOMT
R8TSSBB
R8TSSBN
R8TSSBR
R8TSSBS
R8TSSBT
R8TSSHB
R8TSSHN
R8TSSHR
R8TSSHS
R8TSSHT
R8TSSMB
R8TSSMN
R8TSSMR
Serial Numbers:
All serial numbers affected manufactured from 01/16/2025 to 01/21/2026
UDI (201):
00840331299052
00840331260311
00840331260328
00840331260359
00840331260366
00840331260373
00840331260397
00840331260403
00840331295948
00840331295955
00840331260427
00840331260434
00840331260465
00840331260458
00840331260441
00840331260489
00840331260496
00840331295979
00840331295986
00840331260519
00840331260533
00840331260540
00840331260557
00840331260571
00840331270525
00840331270532
00840331270549
00840331260595
00840331260601
00840331260618
00840331260625
00840331260632
00840331260649
00840331270594
00840331270587
00840331260656
00840331260663
00840331260670
00840331270495
00840331270501
00840331270518
00840331260687
00840331260694
00840331260700
00840331260717
00840331260724
00840331260731
00840331270563
00840331270556
00840331260748
Date Ranges: Manufactured 01/16/2025 to 01/21/2026

Recall #: Z-1753-2026. Quantity: 41,962 units.

Product: Burlington Medical, Vest
Variants: Xenolite 800 attenuation material
Model / REF:
C8PVEST
C8VEST
R8FVEST
R8PVEST
R8QVEST
R8VEST
R8ZVEST
S8FVEST
S8PVEST
S8QVEST
S8VEST
S8ZVEST
U8FVEST
U8PVEST
U8QVEST
U8VEST
U8ZVEST
Serial Numbers:
All serial numbers affected manufactured from 01/16/2025 to 01/21/2026
UDI (158):
00840331297652
00840331297645
00840331259520
00840331259537
00840331259551
00840331259568
00840331259575
00840331259582
00840331259599
00840331259605
00840331259612
00840331259629
00840331259636
00840331259643
00840331259650
00840331269741
00840331269758
00840331259841
00840331259858
00840331259865
00840331259872
00840331259889
00840331259896
00840331259902
00840331259919
00840331259926
00840331259933
00840331259940
00840331259957
00840331259964
00840331259971
00840331259988
00840331269680
00840331269697
00840331260076
00840331260083
00840331260106
00840331260113
00840331260007
00840331269802
00840331260120
00840331261752
00840331261769
00840331261776
00840331261783
00840331261790
00840331261806
00840331261813
00840331261820
00840331261837
Date Ranges: Manufactured 01/16/2025 to 01/21/2026

Recall #: Z-1754-2026. Quantity: 15,438 units.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98415
Status: Active
Manufacturer: Burlington Medical, LLC
Sold By: authorized distributors; healthcare facilities; Burlington Medical
Manufactured In: United States
Units Affected: 13 products (41,962 units; 15,438 units; 15,216 units; 14323; 5,198 units; 1,489 units; 1,129 units; 961 units; 103 units; 402 units; 29 units; 51 units; 94 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.