Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

15476–15500 of 27500

HighFDA (Devices)·Z-2126-2019·2019-08-07
Burlington Medical Recalls Half Aprons Due to Potential Radiation Protection Deficiency
Burlington Medical is recalling two half aprons because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to higher radiation levels.
Product
Half Apron, Product Number Half Apron, Part Numbers REHALF*, REHALF3 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…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2019·2019-08-07
Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection
Burlington Medical is recalling 807 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially increasing long-term health risks.
Product
Thyroid Collar, Buckle Closure, Product Number TS4, Part Numbers RBTS4-R, RBTS4-T2T, RETS4-R, RLTS4-R, RLTS4-SEP, RLTS4-T2T, SBTS4-R, SETS4-T2T, SLTS4-R, UETS4-R Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2128-2019·2019-08-07
Burlington Medical Recalls Radiation Protection Hoods Due to Inadequate Shielding
Burlington Medical is recalling three radiation protection hoods because the protective material may not adequately shield users from scatter radiation.
Product
Hood, Product Number Hood, Part Numbers HOOD1, HOOD2 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.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2124-2019·2019-08-07
Burlington Medical Recalls Frontal Radiation Protection Aprons Due to Inadequate Shielding
Burlington Medical is recalling Frontal Aprons with Quick Drop Velcro Closure because the protective material may provide inadequate protection against scatter radiation.
Product
Frontal Apron with Quick Drop Velcro Closure (no elastic), Product Number 401, Part Numbers RE401*M Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2090-2019·2019-08-07
Encore Medical Recalls Flexible Drill Shafts Due to Manufacturing Error
Encore Medical is recalling 21 Flexible Drill Shafts because a manufacturing error may prevent the shaft from capturing the drill bit pin, potentially causing the bit to come loose during surgery.
Product
Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-2103-2019·2019-08-07
Terumo Capiox NX19 Oxygenator Recalled for Non-Functioning Thermistor
Terumo is recalling 78 Capiox NX19 Oxygenators exported to Japan and Belgium because they may contain a non-functioning arterial thermistor component.
Product
Terumo Capiox NX19 Oxygenator (East Orientation), P/N: CXOT280 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2102-2019·2019-08-07
Terumo Capiox NX19 Oxygenator Recalled for Non-Functioning Thermistor
Terumo is recalling 52 Capiox NX19 Oxygenators because they may contain a non-functioning arterial thermistor component.
Product
Terumo Capiox NX19 Oxygenator With Reservoir (West Orientation) P/N: 3CX*NX19RW
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2120-2019·2019-08-07
Burlington Medical Recalls Radiation Protection Aprons Due to Inadequate Shielding
Burlington Medical is recalling two radiation protection aprons because the protective material may provide inadequate shielding, potentially exposing users to scatter radiation.
Product
1 pc Full Wrap Back Relief Apron, Product Number B52 Front & Back Apron, Part Numbers SEB52*F, UEB52*M Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2123-2019·2019-08-07
Burlington Medical Recalls Radiation Protection Sleeves Due to Inadequate Shielding
Burlington Medical is recalling 39 radiation protection sleeves because the material may provide inadequate protection against scatter radiation.
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 healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2115-2019·2019-08-07
Burlington Medical Recalls Overlap Vests Due to Potential Inadequate Radiation Protection
Burlington Medical is recalling seven Overlap Vests because the protective material may provide inadequate protection against scatter radiation.
Product
Overlap Vest, Single Item, Product Number FVest, Part Numbers REFVEST*F, REFVEST*M, REFVESTE, REFVESTXLM, SEFVEST*F, SEFVEST*M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2116-2019·2019-08-07
Burlington Medical Recalls Lead Apron Products Due to Inadequate Radiation Protection
Burlington Medical is recalling 332 lead apron products because the protective material may provide inadequate protection against scatter radiation.
Product
2 pc Full Wrap Vest & Kilt Back-Saver , Product Number PVK, Part Numbers REPVK*F, REPVK*M, REPVKE, REPVKF, REPVKXLM, SEPVK*F, SEPVK*M, SEPVKE, UEPVK*F Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2107-2019·2019-08-07
Burlington Medical Recalls Frontal Stretch Buckle Closure Aprons
Burlington Medical is recalling nine Frontal Stretch Buckle Closure Aprons because the protective material may provide inadequate protection against scatter radiation.
Product
Frontal Stretch Buckle Closure Apron, Product Number A-10, Part Numbers REA10A, REA10B, REA10C, REA10*F, REA10*M, UEA10*M Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2091-2019·2019-08-07
Elekta Monaco Radiation Treatment Planning System Software Recall
Elekta Inc is recalling Monaco RTP System software versions 5.10 and 5.11 due to a defect that causes incorrect Monitor Unit scaling when specific plan parameters are changed.
Product
Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2109-2019·2019-08-07
Burlington Medical Frontal Support Belt Apron Recalled for Inadequate Radiation Protection
Burlington Medical is recalling six Frontal Support Belt Aprons because the protective material may provide inadequate protection against scatter radiation.
Product
Frontal Support Belt Apron, Product Number F-15, Part Numbers REF15*F, REF15*M, REF15B, REF15XLM Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1956-2019·2019-08-07
Centurion Recalls Sheridan Endotracheal Tubes for Connector Disconnection
Centurion Medical Products is recalling 80 Sheridan Endotracheal Tubes due to an increased incidence of the connector becoming disconnected from the tube.
Product
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2131-2019·2019-08-07
GE Senographe Pristina Mammography Systems Recalled for Biopsy Positioner Slippage
GE Healthcare is recalling 82 Senographe Pristina mammography systems because the biopsy positioner may slip when the gantry is rotated during a procedure.
Product
GE Senographe Pristina - Product Usage: Senographe Pristina generates digital mammographic images that can be used for screening and in the diagnosis of breast cancer. Senographe Pristina is intended to be used in the same clinical applications as traditional film-based…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2110-2019·2019-08-07
Burlington Medical Recalls Frontal Quick Drop OR Aprons Due to Radiation Risk
Burlington Medical is recalling 23 Frontal Quick Drop OR Aprons because the protective material may provide inadequate protection against scatter radiation.
Product
Frontal Quick Drop OR Apron, Product Number 601, Part Numbers ECRE601A, ECRE601B, ECRE601C, ECRE601XLM, RE601*M, RE601C, RE601D, RE601XXLM Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2101-2019·2019-08-07
Terumo Capiox NX19 Oxygenator Recalled for Non-Functioning Arterial Thermistor
Terumo is recalling 16 Capiox NX19 Oxygenators with a non-functioning arterial thermistor component. The units were distributed in Michigan, Japan, and Belgium.
Product
Terumo Capiox NX19 Oxygenator With Reservoir (East Orientation) P/N: 3CX*NX19RE
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2125-2019·2019-08-07
Burlington Medical Recalls Radiation Protection Aprons Due to Inadequate Shielding
Burlington Medical is recalling 48 radiation protection aprons because the protective material may provide inadequate shielding, potentially exposing users to scatter radiation.
Product
Front/Back Apron with Stretch Velcro Closure, Product Number EURO, Part Numbers ECSEEUROA, ECSEEUROB, ECSEEUROC, ECSEEUROXLM, REEURO*F, REEURO*M, REEUROC, REEUROE, SEEURO*F, SEEURO*M, UEEURO*F Product Usage: Products are designed to protect healthcare workers against scatter…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2108-2019·2019-08-07
Burlington Medical Recalls Frontal Apron Velcro Closures Due to Radiation Protection Concerns
Burlington Medical is recalling 104 Frontal Apron Velcro Closures because the protective material may provide inadequate protection against scatter radiation.
Product
Frontal Apron Velcro Closure, Product Number F-17, Part Numbers REF17A, REF17B, REF17C, REF17D, REF17*F, REF17*M, REF17XLF, REF17XLM, REF17XXLM, REF173XLM, UEF17A, UEF17M, UEF17*F, UEF17*M, UEF17XLF, UEF17XXLM Product Usage: Products are designed to protect healthcare…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2121-2019·2019-08-07
Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection
Burlington Medical is recalling 2,190 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to increased health risks.
Product
Thyroid Collar, Velcro Closure, Product Number TS2, Part Numbers RBTS2-R, RETS2-R, RLTS2PED, RLTS2-R, RLTS2-SEP, RLTS2-T2T, SBTS2-R, SETS2-R, SLTS2-R, UETS2-R, UETS2-SEP, ULTS2-R, ULTS2-SEP Product Usage: Products are designed to protect healthcare workers against scatter…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2019·2019-08-07
Wilson-Cook Medical Recalls Acuject Variable Injection Needles
Wilson-Cook Medical is recalling Acuject Variable Injection Needles due to a potential for occluded needles. The affected units were distributed to China.
Product
Acuject Variable Injection Needle
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2132-2019·2019-08-07
GE Pristina Serena Breast Biopsy Accessory Recalled for Slippage Risk
GE Healthcare is recalling 16 Pristina Serena breast biopsy accessories because the positioner may slip when the machine rotates during a procedure.
Product
GE Pristina Serena - Product Usage: Pristina Serena is an optional accessory of Senographe Pristina intended to provide accurate location of lesions in the breast in three dimensions.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2111-2019·2019-08-07
Burlington Medical Recalls Full Wrap Support Belt Aprons Due to Radiation Risk
Burlington Medical is recalling 51 Full Wrap Support Belt Aprons because the protective material may provide inadequate protection against scatter radiation.
Product
1 pc Full Wrap Support Belt Apron, Product Number F111, Part Numbers MTREF111*F, MTREF111E, MTREF111F, REF111*F, REF111*M, REF111B, REF111E, REF111F, SEF111*F, SEF111*M, SEF111C, SEF111D, SEF111E, SEF111F, UEF111*F, UEF111*M, UEF111A, UEF111B, UEF111C, UEF111D, UEF111E…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2117-2019·2019-08-07
Burlington Medical Recalls Seven Peak Vests Due to Inadequate Radiation Protection
Burlington Medical is recalling seven Peak Vests because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to higher radiation levels.
Product
Peak Vest, Single Item, Product Number PVest, Part Numbers REPVEST*M, SEPVESTE, SEPVEST*F Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount…
Category
Medical Device
Distribution
Distributed nationwide

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15476–15500 of 27500