Medical DeviceApr 8, 2026
Burlington Medical, BAT recall — FDA Z-1758-2026
Potential for attenuation degradation over time, decreasing the lifespan.
Class IIFDA: OngoingBurlington Medical, LLC
Recall history in this database
Classification mix: Class II: 25.
Medical DeviceAug 7, 2019
Burlington Medical Frontal Apron with Quick Drop Velcro Closure (no elastic), Product Number recall — FDA Z-2124-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Hood, Product Number Hood, Part Numbers HOOD1, HOOD2 Product Usage recall — FDA Z-2128-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Frontal Apron Velcro Closure, Product Number F-17, Part Numbers REF17A recall — FDA Z-2108-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Frontal Support Belt Apron, Product Number F-15, Part Numbers REF15*F recall — FDA Z-2109-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Overlap Vest, Single Item, Product Number FVest, Part Numbers REFVEST*F recall — FDA Z-2115-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Vest, Single Item, Product Number Vest, Part Numbers ECREVESTD recall — FDA Z-2113-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical 2 pc Full Overlap Vest & Kilt, Single Item, Product Number FVK, Part recall — FDA Z-2114-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Front/Back Apron with Stretch Velcro Closure, Product Number EURO, Part recall — FDA Z-2125-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical 2 pc Full Wrap Vest & Kilt, Product Number VK, Part Numbers ECREVKA recall — FDA Z-2112-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Kilt, Single Item, Product Number Kilt, Part Numbers ECREKILTF recall — FDA Z-2118-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Sleeve, Product Number Sleeve, Part Numbers RESL, SL 3 L, SL 3 M, SL 3 S recall — FDA Z-2123-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Thyroid Collar, Buckle Closure, Product Number TS4, Part Numbers RBTS4-R recall — FDA Z-2122-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R recall — FDA Z-2130-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers recall — FDA Z-2119-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical 2 pc Full Wrap Vest & Kilt Back-Saver , Product Number PVK, Part Numbers recall — FDA Z-2116-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Porta Shield, Product Number Porta Shield, Part Numbers PTS2, PTS3, PTS4 recall — FDA Z-2129-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Frontal Quick Drop OR Apron, Product Number 601, Part Numbers ECRE601A recall — FDA Z-2110-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Half Apron, Product Number Half Apron, Part Numbers REHALF*, REHALF3 recall — FDA Z-2126-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Cap, Product Number Cap, Part Numbers CAP1, CAP2 Product Usage: Products recall — FDA Z-2127-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Peak Vest, Single Item, Product Number PVest, Part Numbers REPVEST*M recall — FDA Z-2117-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical 1 pc Full Wrap Support Belt Apron, Product Number F111, Part Numbers recall — FDA Z-2111-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Thyroid Collar, Velcro Closure, Product Number TS2, Part Numbers RBTS2-R recall — FDA Z-2121-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Medical DeviceAug 7, 2019
Burlington Medical Frontal Stretch Buckle Closure Apron, Product Number A-10, Part Numbers recall — FDA Z-2107-2019
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…
Class IIFDA: TerminatedBurlington Medical, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Burlington Medical, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.