Hazard

Instrument Malfunction recalls

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

What the numbers show

Total: 18
Critical: 0
Severe: 0
Most recent: 2026-04-08

Of the 18 instrument malfunction recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all instrument malfunction 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.

1–18 of 18

HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1699-2026·2026-04-08
da Vinci grasping retractor instruments recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1697-2026·2026-04-08
da Vinci double fenestrated grasper recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Double Fenestrated Grasper Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including bl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1696-2026·2026-04-08
da Vinci monopolar curved scissors recalled over frayed grip cables
Intuitive Surgical is recalling da Vinci S and Si Monopolar Curved Scissors Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1698-2026·2026-04-08
da Vinci mega needle driver recalled over broken or frayed cables
Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2546-2025·2025-09-17
Glenoid reamer heads recalled because they may kick or bind during use
DJO Surgical Altivate Reverse Wedge Glenoid Reamer Heads are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 927 units are affected.
Product
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Product Description: Material: S.S/Nitronic, Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2549-2025·2025-09-17
Shoulder glenoid tray kits recalled because the reamer may kick or bind
DJO Surgical FA S Altivate Reverse Glenoid Tray kits are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 439 kits are affected.
Product
Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version: NA Product Description: Enovis" shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for u
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2547-2025·2025-09-17
Glenoid reamer boss drills recalled because the reamer may kick or bind
DJO Surgical Altivate Reverse Wedge Glenoid Reamer Boss Drills, 6.5 mm, are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 907 units are affected.
Product
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number: 804-06-312 Product Description: Material: S.S., Non Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2548-2025·2025-09-17
Glenoid reamer sleeves recalled over potential for reamer kicking or binding
DJO Surgical Altivate Reverse Wedge Glenoid Reamer Sleeves are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 447 units are affected.
Product
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catalog Number: 804-06-310 Product Description: Material: S.S/CoCrMo, Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0872-2025·2025-01-22
Reusable Surgical Forceps Recall Due to Frayed or Broken Grip Cables
Intuitive Surgical is recalling 1,562 units of 8mm surgical forceps (Model 471048) due to complaints of frayed or broken grip cables. The defect could impair instrument function during use.
Product
8MM,LONG TIP FORCEPS,IS4000 REF 471048
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0857-2025·2025-01-22
Surgical Forceps Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling 373 Resano Forceps due to increased complaints of frayed or broken grip cables on the reusable surgical instruments. Affected healthcare providers should contact the manufacturer for guidance.
Product
8MM,RESANO FORCEPS,IS4000 ¿ REF 470181
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0865-2025·2025-01-22
Reusable Surgical Instruments Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling reusable surgical instruments due to reports of frayed or broken grip cables that may affect safe operation during procedures.
Product
8MM,MEGA SUTURECUT ND,IS4000¿ REF 470309
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0881-2025·2025-01-22
Intuitive Surgical Bipolar Dissector Recalled for Frayed Grip Cables
Intuitive Surgical is recalling 8MM curved bipolar dissectors due to frayed or broken grip cables that could affect surgical instrument performance. Approximately 3,869 units were distributed nationwide and internationally.
Product
8MM,CURVED BIPOLAR DISSECTOR,IS4000 REF 471344
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0852-2025·2025-01-22
Intuitive Surgical DeBakey Forceps Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling 1,739 8MM DeBakey Forceps (Model 470036) used in surgical procedures due to increased reports of frayed or broken grip cables. Cable failure could impair instrument function during surgery.
Product
8MM,DEBAKEY FORCEPS,IS4000 ¿ REF 470036
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0847-2025·2025-01-22
Intuitive Surgical Monopolar Curved Scissors Recalled for Frayed Grip Cables
Intuitive Surgical recalls 355,547 monopolar curved scissors due to increased complaints of frayed or broken grip cables on these reusable surgical instruments.
Product
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0157-2020·2019-10-23
Vital Scientific Selectra ProM Analyzer Recalled for Power Supply Failure
Vital Scientific N.V. is recalling five Selectra ProM Analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.
Product
Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and Catalog # 6003-436/UDI # 03661540600401 Product Usage: :clinical chemistry system intended for use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0158-2020·2019-10-23
Vital Scientific Selectra ProS Analyzer Recalled for Power Supply Failure
Vital Scientific is recalling six Selectra ProS Analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.
Product
Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product Usage: :clinical chemistry system intended for use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide