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.

1–25 of 121

ModerateFDA (Devices)·Z-2319-2026·2026-06-17
Mahurkar Elite PASS trays shipped without the labeled Tegaderm CHG dressing
Mahurkar Elite PASS Trays are being recalled because the Tegaderm CHG dressing specified in the product labeling was missing from certain lots. 25,627 units are affected.
Product
Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter wi
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2354-2026·2026-06-17
Philips DigitalDiagnost C90 delivered without required wall stand seismic kit
A DigitalDiagnost C90 radiography system is being recalled because it was delivered without the seismic kit required for the Wall Stand VS2. One unit is affected.
Product
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1509-2026·2026-03-18
Exactech Ergo modular impactor handle may be missing its cross-pin
Exactech is recalling the Equinoxe Ergo Modular Impactor Handle, model 321-09-05, because the impactor handle may be missing a cross-pin.
Product
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-1510-2026·2026-03-18
Exactech Equinoxe core instrument kits may have handles missing cross-pins
Exactech is recalling the Equinoxe Core Instrument Kit, model KIT-311X, because the impactor handle may be missing a cross-pin.
Product
Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X
Category
Medical Device
Distribution
25 states
ModerateFDA (Drugs)·D-0340-2026·2026-02-18
Cetrorelix injection kits recalled over missing or duplicated needles inside
Meitheal Pharmaceuticals is recalling 16,477 Cetrorelix Acetate for Injection kits over a defective delivery system, with needles either missing from or duplicated within the kit.
Product
CETRORELIX ACETATE — CETRORELIX ACETATE (CETRORELIX ACETATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1298-2026·2026-02-11
Nasal jejunal feeding tubes recalled without the nasal transfer tube
Wilson-Cook Medical is recalling 60 Nasal Jejunal Feeding Tubes, REF NJFT-10, because they were packaged without the nasal transfer tube component.
Product
Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1075-2026·2026-01-21
Allura Xper FD20, model 722028, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20; Model Number: 722028;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1049-2026·2026-01-21
Allura Xper FD20/10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20/10, model 722029, because the drip tray beneath the cooling unit may not have been installed.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1060-2026·2026-01-21
Allura Xper FD10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 56 units of the Allura Xper FD10, model 722010, because the drip tray beneath the cooling unit may not have been installed.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1066-2026·2026-01-21
Allura Xper FD20, model 722006, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 143 units of the Allura Xper FD20, model 722006, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20; Model Number: 722006;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1062-2026·2026-01-21
Allura Xper FD10C systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.
Product
Product Name: Allura Xper FD10C; Model number: 722001;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1077-2026·2026-01-21
Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20/20; Model Number: 722038;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1073-2026·2026-01-21
Allura Xper FD20 Biplane, model 722013, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 23 units of the Allura Xper FD20 Biplane, model 722013, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722026;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1067-2026·2026-01-21
Allura Xper FD20 Biplane systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 18 units of the Allura Xper FD20 Biplane, model 722008, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20 Biplane; Model Number: 722008;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1074-2026·2026-01-21
Allura Xper FD10/10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 22 units of the Allura Xper FD10/10, model 722027, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722027;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1072-2026·2026-01-21
Allura Xper FD20 OR Table recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20 OR Table, model 722023, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20 OR Table; Model Number: 722023;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1017-2026·2026-01-21
Allura Xper FD20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 79 units of the Allura Xper FD20, model 722012, because the drip tray beneath the cooling unit may not have been installed.
Product
VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1069-2026·2026-01-21
Allura Xper FD10/10, model 722011, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 21 units of the Allura Xper FD10/10, model 722011, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722011;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1065-2026·2026-01-21
Allura Xper FD10/10, model 722005, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722005;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1068-2026·2026-01-21
Allura Xper FD10, model 722026, recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 95 units of the Allura Xper FD10, model 722026, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722010;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1063-2026·2026-01-21
Allura Xper FD10F systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 12 units of the Allura Xper FD10F, model 722002, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10F; Model Number: 722002;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1064-2026·2026-01-21
Allura Xper FD10, model 722003, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722003;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26C001000·2026-01-20
Evenflo Recalls Titan 65 Child Seats Missing Tether Straps
Evenflo is recalling specific Titan 65 child seats that may lack a tether strap, which could reduce crash protection and increase injury risk.
Product
CHILD SEAT:TETHER: STRAP/WEBBING recall
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1008-2026·2026-01-07
Laser and endoscopy systems recalled over ferrites omitted from a USB cable
Beaver-Visitec International is recalling 5 BVI Leos Laser and Endoscopy Systems because ferrites specified for the USB cable assembly were not installed as intended.
Product
BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0597-2026·2025-12-17
Fluoroscopy systems recalled after shipping without the source-to-skin distance spacer
Philips is recalling 110 Azurion R3.0 systems shipped with a FlexArm stand but without the Source-to-Skin Distance spacer needed to meet the FDA minimum 38 cm requirement.
Product
Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
Category
Medical Device
Distribution
0 states