State

Puerto Rico product recalls

72,919 recalls have nationwide distribution and so reach Puerto Rico. 3,090 additional recalls listed Puerto Rico specifically in their distribution scope.

What the numbers show

Total: 3,090
Critical: 366
Severe: 625
Most recent: 2026-09-02

Of the 3,090 recalls naming Puerto Rico we have scored against our rubric, 366 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 625 (20%) are Severe.

Which agencies issued them

These figures cover only the 3,090 recalls whose distribution notice names Puerto Rico specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2626–2650 of 76009

HighFDA (Devices)·Z-1642-2026·2026-04-01
Olympus PKS cutting forceps 3005PK jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps model 3005PK because a supplier did not adequately validate the welding process and defective welds can cause the jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualiza
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1643-2026·2026-04-01
Olympus PKS cutting forceps 920000PK jaws may break from welds
Olympus is recalling PKS Cutting Forceps with cord, model 920000PK, because a supplier did not adequately validate the welding process and defective welds can cause the jaw to break.
Product
Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1645-2026·2026-04-01
BD Alaris system labeling omits required TLS version for secure Wi-Fi
CareFusion is recalling the BD Alaris System with Guardrails Suite MX because the product labeling does not indicate which TLS version must be enabled on the hospital network for secure Wi-Fi communication.
Product
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0401-2026·2026-04-01
Sodium iodide capsule packs recalled after failing capsule specifications
Radnostix is recalling three lots of the Gelatin Capsule Pack used with the Sodium Iodide I-131 Kit because the product failed tablet and capsule specifications.
Product
SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2026·2026-04-01
BiDop 3 pocket Doppler labeling includes uncleared fetal indication
Koven Technology is recalling the BiDop 3 Pocket Doppler packaged with a fetal probe because the product labeling includes a fetal indication for use that is not cleared under its 510(k).
Product
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2026·2026-04-01
Philips S4-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the S4-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S4-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the 3D6-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2026·2026-04-01
Philips OMNI III TEE transducer labelling updated to define useful life
Philips is recalling the OMNI III TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI III TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2026·2026-04-01
Philips S5-2 ultrasound transducer labelling updated to define useful life
Philips is recalling one S5-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S5-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1621-2026·2026-04-01
Philips L17-5 ultrasound transducer labelling updated to define useful life
Philips is recalling two L17-5 Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L17-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1619-2026·2026-04-01
Philips C9-4 ultrasound transducer labelling updated to define useful life
Philips is recalling one C9-4 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips C9-4 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1627-2026·2026-04-01
Philips X3-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the X3-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X3-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1628-2026·2026-04-01
Philips X7-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the X7-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X7-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1620-2026·2026-04-01
Philips L12-5 ultrasound transducer labelling updated to define useful life
Philips is recalling the L12-5 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L12-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1622-2026·2026-04-01
Philips Mini Multi TEE transducer labelling updated to define useful life
Philips is recalling the Mini Multi TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips Mini Multi TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1623-2026·2026-04-01
Philips OMNI II TEE transducer labelling updated to define useful life
Philips is recalling two OMNI II TEE Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI II TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V205000·2026-03-31
2026 Ford Explorer and Mustang Engine Piston Circlip Defect Recall
Ford is recalling certain 2026 Explorer and Mustang vehicles because engine piston circlips may have been incorrectly installed, risking loss of drive power and increasing crash risk.
Product
FORD — FORD EXPLORER, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V201000·2026-03-31
2025–2026 Ford Bronco Sport and Maverick Occupant Sensor Recall
Ford is recalling certain 2025–2026 Bronco Sport and Maverick vehicles because the front passenger occupant classification sensor may fail to detect a passenger, risking failure of the airbag to deploy in a crash.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V203000·2026-03-31
Toyota Corolla Cross Hybrid may not sound sufficient pedestrian warning
Toyota is recalling certain 2023-2025 Corolla Cross Hybrid vehicles because they may fail to make sufficient pedestrian warning sounds when in reverse. This fails FMVSS 141.
Product
TOYOTA — TOYOTA COROLLA CROSS HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V204000·2026-03-31
Ford and Lincoln windshield wiper arms may break causing wiper failure
Ford is recalling certain 2021-2023 Lincoln Navigator, Expedition and Super Duty vehicles because the windshield wiper arms may break, causing the wipers to fail.
Product
FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, F-250 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V206000·2026-03-31
Nova Bus Recalls 2024-2025 LFS Models Due to Window Glass Detachment Risk
Nova Bus is recalling 2024 LFS Artic and 2025 LFS transit buses because inadequate window frame adhesion may cause glass to detach, increasing injury and road hazard risks.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V202000·2026-03-31
Ford Recalls 2026 Explorer and Aviator for HVAC Defrost Failure
Ford is recalling 2026 Lincoln Aviator and Explorer vehicles because the HVAC system may fail, causing the windshield defrosting and defogging systems to become inoperative.
Product
FORD — FORD, LINCOLN EXPLORER, AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E017000·2026-03-31
Ricon Power Transfer Seat Bases Recalled for Failure to Lock in Place
Ricon is recalling R1200 series power transfer seat bases because the gear motor may fail to lock the seat, increasing injury risk during a crash.
Product
SEATS:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26E016000·2026-03-30
Terex Recalls Pole Position Guide Arm Assembly Pins Due to Weld Defect
Terex is recalling pole position guide arm assembly pins because an insufficient weld may crack, causing the pin to separate and the arm to fall.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V200000·2026-03-29
Aston Martin DBX rear lower suspension arm may crack or shear
Aston Martin is recalling certain 2021-2026 DBX, DBX707 and DBX S vehicles because the torque reaction link pin may slide out of the rear lower suspension arm, cracking or shearing the arm casting.
Product
ASTON MARTIN — ASTON MARTIN DBX, DBX S, DBX707
Category
Vehicle
Distribution
Distributed nationwide