Hazard

Component Detachment recalls

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

What the numbers show

Total: 189
Critical: 0
Severe: 57
Most recent: 2026-08-19

Of the 189 component detachment recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 57 (30%) 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 component detachment 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.

126–150 of 189

HighFDA (Devices)·Z-2267-2020·2020-06-17
Genicon GENILook Medical Device Recalled Due to Detachment Risk
Genicon, Inc. is recalling GENILook Model 200-005-152 medical devices because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-005-152, 5mm diameter, 100mm legnth (2 cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2274-2020·2020-06-17
Genicon Natura Cannula Recall Due to Detachable Optical Tip
Genicon, Inc. is recalling Natura Model 210-005-151 cannulas because the plastic optical tip may detach from the metal shaft.
Product
Genicon Natura Model 210-005-151; 5mm diameter, 100mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2271-2020·2020-06-17
Genicon GENILook Medical Device Recalled Due to Detached Optical Tip Risk
Genicon, Inc. is recalling GENILook Model 200-105-152 devices because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-105-152, 5mm diameter, 100mm length (2 cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2270-2020·2020-06-17
Genicon GENILook Cannula Recalled Due to Potential Tip Detachment
Genicon, Inc. is recalling GENILook Model 200-105-151 cannulas because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-105-151, 5mm diameter, 100mm length (one cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2275-2020·2020-06-17
Genicon Natura Trocar Handle Recall Due to Detaching Optical Tip
Genicon, Inc. is recalling Natura Model 210-005-152 trocar handles because the plastic optical tip may detach from the metal shaft.
Product
Genicon Natura Model 210-005-152, 5mm diameter, 100mm length (two cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2266-2020·2020-06-17
Genicon GENILook Cannula Recalled for Potential Tip Detachment
Genicon, Inc. is recalling GENILook cannulas because the plastic optical tip may detach from the metal shaft. The recall affects 378 boxes distributed in the US and abroad.
Product
Genicon GENILook Model 200-005-151, 5mm diameter, 100mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2269-2020·2020-06-17
Genicon GENILook Cannula Recalled for Potential Tip Detachment
Genicon, Inc. is recalling GENILook Model 200-005-251 cannulas because the plastic optical tip may detach from the metal shaft.
Product
Genicon GENILook Model 200-005-251, 5mm diameter, 150mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-2276-2020·2020-06-17
Genicon Natura Cannula Recalled Due to Potential Tip Detachment
Genicon, Inc. is recalling Natura Model 210-005-251 cannulas because the plastic optical tip may detach from the metal shaft.
Product
Genicon Natura Model 210-005-251, 5mm diameter, 150mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-1858-2020·2020-05-13
R82 A/S Recalls Chest Supports for Loose Plastic Plug
R82 A/S is recalling 2,230 chest supports for the R82 Mustang and Rabbit Up because a plastic plug can come loose without tools.
Product
Chest Support for R82 Mustang, Model Numbers: 861810, 861820, 861830; and Rabbit Up, Model Numbers: 869810, 869820, 869830
Category
Medical Device
Distribution
1 state
SevereNHTSA·20V075000·2020-02-12
Forest River Recalls 2019-2020 Trailers Due to Spare Tire Carrier Defect
Forest River is recalling 2019-2020 trailers because spare tire carrier U-bolts may fail, allowing the tire to detach and create a road hazard.
Product
FOREST RIVER — FOREST RIVER, COACHMEN INDEPENDENCE, R-POD, VIKING, PUMA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V462000·2019-06-14
Caterpillar Recalls 2015-2019 Progress Rail Sky Trim Hi-Rail Vehicles
Caterpillar is recalling 2015-2019 Progress Rail Sky Trim Hi-Rail vehicles because a support plate may block driver visibility and the boom may detach from the cradle while in motion.
Product
PROGRESSIVE RAIL SERVICES — PROGRESSIVE RAIL SERVICES SKY TRIM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1058-2019·2019-04-03
Sunset Compressor Nebulizer Recalled for Overheating and Mouthpiece Detachment Risk
SANRAI INTERNATIONAL LLC is recalling 150 Sunset Compressor Nebulizer units in South Africa due to voltage incompatibility risks.
Product
Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-powered air nebulizer compressor system intended to provide a source of compressed air for medical purposes for use in home healthcare. It is to be used with a nebulizer kit to pro
Category
Medical Device
Distribution
0 states
HighNHTSA·18V752000·2018-10-25
Forest River Cherokee Recalled for Insufficient Awning Fasteners
Forest River is recalling 2018-2019 Cherokee Alpha Wolf and 2019 Arctic Wolf trailers because awning fasteners may be insufficient, risking arm detachment.
Product
FOREST RIVER — FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2660-2018·2018-08-15
Arjohuntleigh Magog Quick Connect 272 KG Scale Recall for Detachment Risk
Arjohuntleigh Magog is recalling Quick Connect 272 KG Scales used with Maxi Sky 2 ceiling lifts because the spreader bar can detach from the scale attachment.
Product
Quick Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospitals, nursing homes, home care or health care facilities
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2605-2018·2018-08-15
Think Surgical Cutter Recall Due to Potential Head Detachment
Think Surgical is recalling 951 flat cutters used in total knee arthroplasty because the cutter head may detach from the shaft.
Product
Think Surgical Cutter, Flat, ¿6.2mm x 144mm. For use only with the TCAT Computer-Assisted Tool. Part Number 106428 The cutter is used to prepare the bone for the (TKA) Total Knee Arthroplasty.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-2148-2018·2018-06-20
Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk
Sun Med, LLC is recalling 5 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially detaching during use and impacting air delivery.
Product
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, FILTER, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1116FC
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2149-2018·2018-06-20
Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk
Sun Med, LLC is recalling 80 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially causing the port to detach and impacting air delivery.
Product
MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1116P
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1781-2018·2018-05-16
Ninepoint Medical Recalls NvisionVLE Low-Profile Optical Probes
Ninepoint Medical is recalling 152 NvisionVLE Low-Profile Optical Probes because the distal tips may detach from the probe shaft during use.
Product
NvisionVLE¿ Low-Profile Optical Probe; Catalog Numbers: 95501-LP and 95501-LP-5; UDI Information: (01)00859591006188(17)180531(10)005196), (01)00859591006188(17)180731(10)005251), (01)00859591006188(17)180930(10)005275) Product Usage: The NvisionVLE Low-Profile Optical Pro
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V202000·2018-03-28
REV Recalls Motorhomes Due to Potential Satellite Dish Detachment
REV is recalling 2017-2018 motorhomes because satellite dish mounting screws may not be fastened correctly, posing a crash risk if the dish detaches.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, AMERICAN COACH, FLEETWOOD PRODIGY, AMERICAN EAGLE, NAVIGATOR, PULSE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V187000·2018-03-22
Keystone Recalls 2018 Passport Trailers Due to Spare Tire Carrier Defect
Keystone RV Company is recalling 2018 Passport recreational trailers because the spare tire carrier may detach, increasing crash risk.
Product
KEYSTONE — KEYSTONE PASSPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0244-2018·2017-12-20
Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.
Product
Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, UPN H965458180, Catalog No. 45-818 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system fo
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0241-2018·2017-12-20
Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included Greatbatch introducer sheaths have handles that may detach during use.
Product
XCELA PASV 5F DL 55CM IR-145 Nitinol Wire KIT PG, UPN H965251260, Catalog No. 25-126 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous syst
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0242-2018·2017-12-20
Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment
Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.
Product
XCELA PASV 5F DL 55CM MST-70 KIT PG, UPN H965457320, Catalog No. 45-732 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system for intrav
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0247-2018·2017-12-20
Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.
Product
Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, UPN H965458710, Catalog No. 45-871 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0240-2018·2017-12-20
Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment
Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.
Product
Xcela PICC Kit with ENDEXO and PASV Valve Technology, XCELA PASV 5F DL 55CM MST-70 Nitinol KIT PG, UPN H965251250, Catalog No. 25-125 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-
Category
Medical Device
Distribution
Distributed nationwide