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U.S. Department of Health and Human Services

Class 2 Device Recall Thyroid Collar

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  Class 2 Device Recall Thyroid Collar see related information
Date Initiated by Firm June 07, 2019
Date Posted July 30, 2019
Recall Status1 Terminated 3 on April 28, 2023
Recall Number Z-2119-2019
Recall Event ID 83144
Product Classification Apron, leaded - Product Code EAJ
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.
Code Information 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 418410 383157 419299 408500 409998 418182 419378 388168 419025 420496 379203 379200 440827 441231 409999 383155 383156 383128 383127 419111 388169 378522 383133 383125 383350 419056 419027 433360 383161 414835 388171 440824 433311 441125 427541 443683 443674 441198 441055 415974 431461 408279 408276 418452 418448 441197 418180 424963 419374 433312 408422 379225 419118 419297 414832 408280 379206 441232 443676 418181 383162 414833 422374 418178 443675 441227 443677 443678 433316 443671 408383 418348 418347 383061 443684 419023 419376 419117 379226 379214 418450 440880 407618 378574 378577 378576 415000 
Recalling Firm/
Manufacturer		 Burlington Medical, LLC
PO Box 3194
3 Elmhurst St
Newport News VA 23603-1137
For Additional Information Contact John Daspit
757-968-5846
Manufacturer Reason
for Recall		 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.
FDA Determined
Cause 2		 Under Investigation by firm
Action Urgent Medical Device Recall notification letters were sent to customers on 6/7/19. Please take the following actions: Cease using recalled products immediately, quarantine the products, and prepare the products for return shipment to Burlington Medical. Contact Burlington Medical at (800) 221-3466 for specific return instructions. Note that Burlington Medical Customer Care will work with you to facilitate the return of recalled products, including by issuing you a Recall Tracking number. Burlington Medical will replace all recalled products at no cost to you. The replacement product will be the same size and model as the recalled product; if the same size and model is not available or has been discontinued, then Burlington Medical will replace the recalled product with a Burlington Medical product that is similar to the recalled product. Our Customer Care team will arrange for free shipment of the replacement product. If you have any questions, please call your Burlington Medical representative or Burlington Medical Customer Care at (800) 221-3466. The recall was expanded an additional Urgent Medical Device Recall notification letters were sent to customers on 7/3/19.
Quantity in Commerce 210
Distribution US Nationwide distribution. The products were distributed to the following foreign countries: Korea, Thailand.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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