Hazard

Missing Component recalls

121 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 121
Critical: 1
Severe: 9
Most recent: 2026-06-17

Of the 121 missing component recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (7%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all missing component recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

51–75 of 121

ModerateFDA (Devices)·Z-2779-2020·2020-08-19
HealthFirst STAT KIT Z-1000 Emergency Medical Kits Recalled for Missing Component
HF Acquisition Co. LLC is recalling two STAT KIT Z-1000 emergency medical kits because they are missing a hand suction pump component.
Product
STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2797-2020·2020-08-19
Wright Medical Screw Removal Case Assembly Recalled for Missing Drivers
Wright Medical Technology is recalling 9 units of the Screw Removal Case Assembly because the kits do not include drivers required to remove specific headless screws.
Product
Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles a
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2796-2020·2020-08-19
Wright Medical Hardware Removal Kit Recalled for Missing Drivers
Wright Medical Technology is recalling 66 hardware removal kits because they lack the specific drivers needed to remove Dart-Fire 2.5 and 3.0mm Headless screws.
Product
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a ra
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2702-2020·2020-08-05
Smith & Nephew T-F1X0 RCG Drill Pac Recalled for Missing Sleeve
Smith & Nephew is recalling T-F1X0 RCG Drill Pacs because some sterile packages contain only one sleeve instead of two, preventing the device from performing as intended for the second bone tunnel.
Product
Smith & Nephew T-F1X0 RCG Drill Pac, 2 mm Drill & (2) Sleeves - Product Usage: indicated for use in surgical arthroscopic rotator cuff repair procedures. REF/ Catalog Number : 014771
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1615-2020·2020-04-08
Biomet Shoulder Baseplate Recall Due to Incorrect Packaging Contents
Biomet is recalling 21 units of Comprehensive Reverse Shoulder Glenosphere Mini Baseplates because some packages contained two baseplates and no taper adapters.
Product
Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder replacement for the relief of pain and significant disability due to gross rotator cuff deficiency Item Number: 010000589
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1402-2020·2020-03-04
MicroVention HydroFrame 10 Embolic Coils Recalled for Missing Implant Coil
MicroVention is recalling 991 HydroFrame 10 and HydroCoil embolic systems because the implant coil may be missing. The devices were distributed outside the United States.
Product
MicroVention Terumo HydroFrame 10, HydroCoil Embolic System, Endovascular Embolization Coil, Sterile, Rx, REF numbers 100306HFRM-V, 100405HFRM-V, 100408HFRM-V, 100410HFRM-V, 100412HFRM-V, 100415HFRM-V, 100510HFRM-V, 100515HFRM-V, 100519HFRM-V, 100612HFRM-V, 100619HFRM-V, 100623HF
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1406-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 666 units of Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex, Platinum Coil System, Endovascular Embolization Coil, VFC, Sterile, Rx, REF numbers MV-00306VFC, MV-00315VFC, MV-00310VFC, MV-00630VFC, VFC010303-V, VFC030606-V, VFC030610-V, VFC030615-V, VFC061020-V, VFC061030-V, VFC101530-V, VFC101540-V, VFC1520
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1403-2020·2020-03-04
MicroVention HydroFrame 18 Embolic System Recalled for Missing Implant Coil
MicroVention is recalling 32 units of HydroFrame 18 embolic systems because the implant coil may be missing. The devices were distributed internationally.
Product
MicroVention Terumo HydroFrame 18, HydroCoil Embolic System, Endovascular Embolization Coil, Sterile, Rx, REF numbers 180723HFRM-V, 180931HFRM-V, 181644HFRM-V, MV-80619HHFA, MV80827HHFA, MV-80931HHFA, and MV-81036HHFA. Product Usage: The HES is also intended for vascular occlu
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1397-2020·2020-03-04
MicroVention Platinum Coil System Recall for Missing Implant Coils
MicroVention is recalling 169 units of Microplex 18 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Helical 18 Soft, Sterile, Rx, REF numbers 180204HC-S-V, 180208HC-S-V, 180308HC-S-V, 180410HC-S-V, and 180512HC-S-V. Product Usage: The MCS is also intended for vascular occlusion of blood v
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1398-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 3,442 units of Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Cosmos 10, Sterile, Rx, REF numbers 100202CSSR-V, 100254CSSR-V, 100306CSSR-V, 100408CSSR-V, 100412CSSR-V, 100515CSSR-V, 100522CSSR-V, 100618CSSR-V, 100626CSSR-V, 100722CSSR-V, 100731CSSR-V,
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1407-2020·2020-03-04
MicroVention Platinum Coil System Recall for Missing Implant Coils
MicroVention is recalling Microplex 10 Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft Helical, Sterile, Rx, REF numbers 100101HS-V, 100102HS-V, 100103HS-V, 100104HS-V, 100151HS-V, 100152HS-V, 100153HS-V, 100154HS-V, 100201HS-V, 100202HS-V, 100203HS-V, 100204HS-V, 100
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1400-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling Microplex 10 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Complex 10, Sterile, Rx, REF numbers 100204CC-V, 100307CC-V, 100410CC-V, 100512CC-V, 100615CC-V, 100718CC-V, 100820CC-V, 100924CC-V, and 101026CC-V. Product Usage: The MCS is also intended
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1395-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention, Inc. is recalling 780 units of Microplex 10 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Helical 10 Soft, Sterile, Rx, REF numbers 100206HCSR-S-V, 100208HC-S-V, 100208HCSR-S-V, 100306HCSR-S-V, 100308HCSR-S-V, 100310HC-S-V, 100310HCSR-S-V, 100410HC-S-V, 100410HCSR-S-V, Product
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1393-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 1,725 units of Microplex 10 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D, Sterile, Rx, REF numbers 100102HS3D-V, 100103HS3D-V, 100152HS3D-V, 100153HS3D-V, 100154HS3D-V, 100202HS3D-V, 100203HS3D-V, 100204HS3D-V, 100206HS3D-V, 100208HS3D-V, 100254HS3D-V
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1394-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 486 units of Microplex 10 Platinum Coil Systems because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Helical 10 Regular, Sterile, Rx, REF numbers 100515HC-R-V, 100515HCSR-R-V, 100520HC-R-V, 100520HCSR-R-V, 100620HC-R-V, 100620HCSR-R-V, 100730HC-R-V, 100730HCSR-R-V, 100830HC-R-V, 100930HC-R-V
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1401-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 19 units of the Microplex 18 Platinum Coil System because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Complex 18, Sterile, Rx, REF numbers 180512CC-V, 180820CC-V, 181026CC-V, 181434CC-V, and 182050CC-V. Product Usage: The MCS is also intended for vascular occlusion of blood vessels within t
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1392-2020·2020-03-04
MicroVention HydroSoft 10 Embolic Coils Recalled for Missing Implant Coil
MicroVention is recalling 2,762 units of HydroSoft 10 embolic coils because the implant coil may be missing from the packaging.
Product
MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, Helical, Sterile, Rx, REF numbers 100101H2HS-V; 100102H2HS-V, 100103H2HS-V, 100104H2HS-V, 100151H2HS-V; 100152H2HS-V; 100153H2HS-V; 100154H2HS-V; 100201H2HS-V; 100202H2HS-V; 100203H2HS-V;
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1399-2020·2020-03-04
MicroVention Platinum Embolization Coils Recalled for Missing Implant Coil
MicroVention is recalling 403 units of Platinum Embolization Coils because the implant coil may be missing from the device.
Product
MicroVention Terumo Microplex 18, Platinum Embolization Coil, Cosmos 18, Sterile, Rx, REF numbers 180619CS-V, 180723CS-V, 180827CS-V, 180931CS-V, 181036CS-V, 181139CS-V, 181243CS-V, 181347CS-V, 181451CS-V, 181652CS-V, 181859CS-V, 182065CS-V, 182263CS-V, and 182468CS-V; Produc
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1396-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coil
MicroVention is recalling 9 units of Microplex 18 Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Helical 18 Regular, Sterile, Rx, REF numbers 180520HC-R-V and 181230HC-R-V. Product Usage: The MCS is also intended for vascular occlusion of blood vessels within the neurovascular system
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1404-2020·2020-03-04
MicroVention Platinum Coil System Recalled for Missing Implant Coils
MicroVention is recalling 85 units of Microplex 10 Platinum Coil Systems because the implant coil may be missing from the packaging.
Product
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Compass 10, Sterile, Rx, REF numbers 100203CMSR-V, 100408CMSR-V, 100412CMSR-V, 100510CMSR-V, 100516CMSR-V, 100612CMSR-V, 100618CMSR-V, and 100721CMSR-V. Product Usage: The MCS is also inten
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1405-2020·2020-03-04
MicroVention HydroSoft Embolization Coils Recalled for Missing Implant Coils
MicroVention is recalling 847 HydroSoft embolization coils because the implant coil may be missing from the packaging. The devices were distributed to 43 countries outside the United States.
Product
MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, HydroSoft 3D, Sterile, Rx, REF numbers 100102HFRM-V, 100152HFRM-V, 100153HFRM-V, 100154HFRM-V, 100202HFRM-V, 100206HFRM-V, 100208HFRM-V, 100254HFRM-V, 100256HFRM-V, 100308HFRM-V, MV-00202
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-1223-2020·2020-02-19
Microvention AZUR Peripheral Coil System Recall for Missing Implant Coil
Microvention is recalling 392 units of AZUR Peripheral Coil Systems because the implant coil may be missing from the devices.
Product
Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil Embolization System, REF numbers 45-451015, 45-451020, 45-451215, 45-451220, 45-451230, 45-451520, 45-451530, 45-452020, 45-452030, 45-450410, 45-450415, 45-450405, 45-450610, 45-450615, 45-450620, 45-450815, 4
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1220-2020·2020-02-19
Terumo AZUR Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 445 units of Terumo AZUR Peripheral Coil Systems because the implant coil may be missing from the device.
Product
Terumo AZUR Peripheral Coil System, Detachable 18, Helical HydroCoil Embolization System, REF numbers 45-481015, 45-481020, 45-481215, 45-481220, 45-481515, 45-481520, 45-482020, 45-482030, 45-480202, 45-480204, 45-480310, 45-480302, 45-480305, 45-480410, 45-480415, 45-480420, 45
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1222-2020·2020-02-19
Terumo AZUR CX Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 3,881 units of the Terumo AZUR CX Peripheral Coil System because the devices may be missing the implant coil.
Product
Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers 45-781032, 45-781238, 45-781434, 45-781639, 45-781836, 45-782040, 45-780202, 45-780204, 45-780304, 45-780308, 45-780413, 45-780516, 45-780620, 45-780724, 45-780828, 45-780928, MV-AX80202CL, MV-AX80204CL, M
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1224-2020·2020-02-19
Terumo AZUR Peripheral Coil System Recalled for Missing Implant Coil
Microvention, Inc. is recalling 19 units of Terumo AZUR Peripheral Coil Systems because the implant coil may be missing from the device.
Product
Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers 45-651026 and 45-652050, Sterile, Rx. The firm name on the label is MicroVention, Inc., Tustin, CA; Distributed By: Terumo Medical Corporation, Somerset, NJ; Made in Costa Rica.
Category
Medical Device
Distribution
1 state