FDA Device recall Z-2119-2019
Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers RBTS5-R, RBTS5-T2T, RLTS5-R, RLTS5-T2T, SLTS5-R Product Usage: Products…
- FDA Device
- Class II
- terminated
- Published 2019-08-07
On 2019-08-07 the FDA classified a Class II recall of Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers RBTS5-R, RBTS5-T2T, RLTS5-R, RLTS5-T2T, SLTS5-R Product Usage: Products… by Burlington Medical, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2119-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-07 |
| Published | 2019-08-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Burlington Medical |
| Distribution | US |
Product
Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers RBTS5-R, RBTS5-T2T, RLTS5-R, RLTS5-T2T, SLTS5-R Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.
Reason
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.
Identifiers
| code_info | Serial Numbers: 419121 443916 408275 419300 419026 418172 418354 418174 418350 418362 418357 414627 418364…Serial Numbers: 419121 443916 408275 419300 419026 418172 418354 418174 418350 418362 418357 414627 418364 418363 418176 418358 418353 418352 418351 418349 418355 418359 418171 418175 418356 379202 418360 383132 414631 419298 408499 408495 429803 408423 408355 383130 424076 378575 378519 427547 419022 419028 419021 383160 414632 408413 408277 419024 383332 376923 378521 378520 383131 379205 419116 415973 409388 409389 408429 408418 422377 379201 379207 409387 409390 379199 414630 414629 418345 418361 418344 418438 418431 418177 443920 440828 433315 379161 379213 414834 441233 443685 407663 408415 408426 408425 408424 433368 441226 408496 418346 443682 433337 418407 383348 383347 414625 422460 414624 414635 383158 419379 419120 408416 418405 419377 383349 419375 383129 383126 419380 414831 414626 424075 383263 414634 383062 414633 379162 379227 379224 408278 441210 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2119-2019%22
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