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.

1–25 of 189

ModerateFDA (Devices)·Z-2917-2026·2026-08-19
Galt Medical Recalls Boston Scientific Transcarotid Access Kits
Galt Medical Corporation is recalling 114,260 Boston Scientific Enhance Transcarotid/Peripheral Access Kits because black depth markings may detach from the outer sheath.
Product
Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/ Radiopaque Tip [Au}, Needle, Extension Tube with Stopcock
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2449-2026·2026-06-24
HarmonyAIR A-Series surgical light intensity control buttons may detach
HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 2,101 units affected.
Product
HarmonyAIR A-Series Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2450-2026·2026-06-24
ALYON surgical light head intensity control buttons may detach
ALYON Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 549 units are affected.
Product
ALYON Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V336000·2026-05-26
Forest River trailer shock bolts may break and detach onto the road
Forest River is recalling certain recreational trailers with Curt Touring Coil Suspensions because shock bolts may have been incorrectly tightened and can break and detach.
Product
FOREST RIVER — FOREST RIVER RIVERSTONE, R-POD, CEDAR CREEK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V299000·2026-05-12
Ford Bronco hardtop roof panel sections may separate and detach
Ford is recalling certain 2021-2022 Bronco vehicles because Molded-In-Color hardtop roof panels may have been manufactured improperly, allowing outer sections to detach.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V276000·2026-04-30
Grand Design Lineage solar panels may detach from the roof
Grand Design is recalling certain 2025-2026 Lineage recreational vehicles because the adhesive securing the roof solar panels may fail, allowing a panel to detach into the roadway.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26457·2026-04-30
Build-A-Bear Heartwarming Hugs bear pouch zipper sliders can detach
Build-A-Bear Workshop Heartwarming Hugs Bears are recalled because the zipper slider on the side pouch can detach, posing a choking hazard to children. About 36,000 units are affected.
Product
Build-A-Bear Workshop Heartwarming Hugs Bears
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1852-2026·2026-04-29
Olympus Thunderbeat II shears 25 cm may shed a distal tip component
Olympus is recalling Thunderbeat II Shears with Ultrasonic Mode, 5 mm and 25 cm, because a distal tip component may detach during use. 365 units are affected.
Product
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 25cm. Model Number: TB2-0525FC.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1853-2026·2026-04-29
Olympus Thunderbeat II shears 35 cm may shed a distal tip component
Olympus is recalling Thunderbeat II Shears with Ultrasonic Mode, 5 mm and 35 cm, because a distal tip component may detach during use. 3,360 units are affected.
Product
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 35cm. Model Number: TB2-0535FC.
Category
Medical Device
Distribution
0 states
HighFDA (Drugs)·D-0441-2026·2026-04-15
Fagron vancomycin 1.5 gram bags recalled over sterility and detaching port part
Fagron is recalling Vancomycin HCl 1.5 grams in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.
Product
Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0438-2026·2026-04-15
Fagron norepinephrine infusion bags recalled over sterility and detaching port part
Fagron is recalling norepinephrine bitartrate 16 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.
Product
norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1774-2026·2026-04-15
Molded Products Luer cap sets recalled after threaded sleeve detachment complaint
Molded Products is recalling the MPC-130 See Luer Cap Set following a confirmed complaint that the threaded sleeve was not engaged and became detached. 26,900 units are affected.
Product
See Luer Cap Set, MPC-130, set, administration, intravascular
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1804-2026·2026-04-15
Stryker tourniquet cuffs may detach from the bladder welding connection
Stryker Sustainability Solutions is recalling Color Cuff tourniquet cuffs because the cuff can detach from the bladder at the welding connection, leaving it unable to maintain pressure.
Product
Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red)
Category
Medical Device
Distribution
41 states
HighFDA (Drugs)·D-0442-2026·2026-04-15
Fagron vancomycin infusion bags recalled over sterility and detaching port part
Fagron Sterile Services is recalling Vancomycin HCl 1 gram in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.
Product
Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0440-2026·2026-04-15
Fagron vancomycin 1.25 gram bags recalled over sterility and detaching port part
Fagron is recalling Vancomycin HCl 1.25 grams in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.
Product
Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0439-2026·2026-04-15
Fagron norepinephrine 32 mg bags recalled over sterility and port part
Fagron is recalling norepinephrine bitartrate 32 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.
Product
norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·26385·2026-04-09
BISSELL steam cleaner attachments can detach and expel hot water
BISSELL Steam Shot OmniReach and Omni handheld steam cleaners are recalled after 206 reports of hot water or steam escaping from the attachments, including 161 reports of burn injuries.
Product
Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26393·2026-04-09
SCUBAPRO weight pocket D-ring handles can detach during a dive
SCUBAPRO Monorail Weight Pockets are recalled because the D-ring handle used to release the pocket from a buoyancy compensator can detach, preventing weight ditching in an emergency.
Product
SCUBAPRO Monorail Weight Pockets for BCDs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1572-2026·2026-03-25
Stryker sagittal saw attachment cover screws may loosen and detach
Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.
Product
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2026·2026-03-18
Link Endo-Model SL connection component recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/07 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1523-2026·2026-03-18
Link Endo-Model plateau 15-0027/16 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/16 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/16;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1522-2026·2026-03-18
Link Endo-Model plateau 15-0027/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2026·2026-03-18
Link Endo-Model plateau 15-8521/09 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/09 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/09;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2026·2026-03-18
Link Endo-Model plateau 15-8030/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8030/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8030/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2026·2026-03-18
Link Endo-Model plateau 15-2835/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2835/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2835/12;
Category
Medical Device
Distribution
Distributed nationwide