The Recall Desk

State

Puerto Rico product recalls

73,570 recalls have nationwide distribution and so reach Puerto Rico. 3,094 additional recalls listed Puerto Rico specifically in their distribution scope.

What the numbers show

Total
3,094
Critical
366
Severe
726
Most recent
2026-09-23

Of the 3,094 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 726 (23%) are Severe.

These figures cover only the 3,094 recalls whose distribution notice names Puerto Rico specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

201–225 of 76664

  • SevereCPSC·27021·2026-10-08

    Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks

    Snow Peak is recalling Takibi propane fireplace inserts and lava rocks because the rocks can ignite and explode, posing burn and fire hazards.

    Product
    Snow Peak Takibi Fireplace Propane Inserts and Lava Rocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V663000·2026-10-08

    Honda Recalls Hybrid and Fuel Cell Vehicles for Tire Repair Kit Defect

    Honda is recalling 2023-2026 CR-V Hybrid, Accord Hybrid, and 2025 CR-V Fuel Cell EV vehicles because the tire repair kit bottle cap may detach and become a projectile.

    Product
    HONDA — 2024 HONDA ACCORD HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1406-2026·2026-10-07

    Todd's Seeds Sprouting Seed Mix Recalled for E. coli and Salmonella Risk

    Todd's Seeds LLC is recalling Sprouting Seed Mix containing alfalfa due to potential contamination with E. coli and Salmonella.

    Product
    Todd's Seeds Sprouting Seed Mix - Broccoli, Radish, Alfalfa, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., and 5 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1407-2026·2026-10-07

    Todd's Seeds Salad Sprouting Mixture Recalled for E. coli and Salmonella Risk

    Todd's Seeds LLC is recalling Salad Sprouting Mixture because it contains alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella.

    Product
    Todd's Seeds Salad Sprouting Mixture - Broccoli, Mustard, Alfalfa and Cabbage, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., and 1 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1409-2026·2026-10-07

    Todd's Seeds Variety Pack Recalled for Potential E. coli and Salmonella Contamination

    Todd's Seeds LLC is recalling a variety pack of sprouting seeds because the alfalfa component may be contaminated with E. coli or Salmonella.

    Product
    Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli, Alfalfa, Radish Mung & Clover, packaged as a multi-pack consisting of 2 oz. heat-sealed resealable bags each
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1408-2026·2026-10-07

    Todd's Seeds Alfalfa and Mung Bundle Recalled for E. coli and Salmonella Risk

    Todd's Seeds LLC is recalling Alfalfa & Mung Bundles because the alfalfa seed may be contaminated with E. coli and/or Salmonella.

    Product
    Todd's Seeds Alfalfa & Mung Bundle (1lb each), packaged separately in heat-sealed resealable bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1404-2026·2026-10-07

    Todd's Seeds Alfalfa Sprouting Seeds Recalled for E. coli and Salmonella

    Todd's Seeds LLC is recalling alfalfa sprouting seeds due to potential contamination with E. coli and Salmonella. The recall is nationwide.

    Product
    Todd's Seeds Alfalfa Sprouting Seeds, packaged in heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., 2.5 lb., and 5 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1405-2026·2026-10-07

    Todd's Seeds Broccoli & Friends Sprouting Seed Mix Recalled for Contamination

    Todd's Seeds LLC is recalling Broccoli & Friends Sprouting Seed Mix because it contains alfalfa seed that may be contaminated with E. coli and/or Salmonella.

    Product
    Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa, Radish, Clover, packaged in 1 oz. sample packets and heat-sealed resealable bags in the following sizes: 1/4 lb., 1/2 lb., 1 lb., 2.5 lb., and 5 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3276-2026·2026-10-07

    Volcano Corp Recalls Philips IntraSight Plus Systems Due to Data Error

    Volcano Corp is recalling 19 Philips IntraSight Plus systems because software may incorrectly associate patient image data with the wrong medical record.

    Product
    Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3227-2026·2026-10-07

    Medline Homecare Bed Hand Pendants Recalled for Fire Hazard

    Medline is recalling specific homecare bed hand pendants because the pendant or wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire.

    Product
    Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/ MDR107003E MDR530094 PENDANT, W/ 9V BATTERY BACKUP, F/ 2E BED MDR540094 PENDANT, W/ 9V BATTERY BACKUP, F/ 3E BED
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3328-2026·2026-10-07

    Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk

    Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers due to a risk of blood-to-glycol leaks during cardiopulmonary bypass procedures.

    Product
    Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 Model/Catalog Number: HX55W-S0 Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V659000·2026-10-07

    Toyota Recalls 2026 RAV4 Plug-In Hybrids for Powertrain Shutdown Risk

    Toyota is recalling 30,978 2026 RAV4 Plug-In Hybrid vehicles because a software error may cause the hybrid system to reduce power or shut down at higher speeds, increasing crash risk.

    Product
    TOYOTA — 2026 TOYOTA RAV4 PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V660000·2026-10-07

    Freightliner and FCCC Trucks Recalled for Fuel Hose Separation Risk

    Daimler Trucks North America is recalling certain Freightliner and FCCC trucks because fuel hoses may separate, causing leaks, engine stalls, and fire risks.

    Product
    FCCC — FCCC, FREIGHTLINER XBS, XCR, XCS, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3327-2026·2026-10-07

    Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk

    Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers because a defect may cause blood to leak into the glycol heat transfer fluid.

    Product
    Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog Number: HX55V-S0W Software Version: N/A Product Description: The Quantum PureFlow Standard Heat Exchanger is intended to be used with a compatible Heater/Cooler…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3228-2026·2026-10-07

    Medline Homecare Beds Recalled for Fire Hazard in Hand Control Pendant

    Medline Industries is recalling Basic and Medlite Homecare Beds due to a potential fire hazard involving the hand control pendant and wiring.

    Product
    Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3252-2026·2026-10-07

    Draeger VentStar Resus Neo Neonatal Breathing Circuit Recall

    Draeger is recalling VentStar Resus Neo neonatal breathing circuits due to potential hose cracks that could cause leakage or disconnection.

    Product
    VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a resuscitation module.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V658000·2026-10-07

    BMW Recalls 2021-2024 R 18 Motorcycles for Fire Risk

    BMW is recalling 2021-2024 R 18 motorcycles with optional reverse gear because a deteriorating seal may allow moisture to enter the control unit, causing overheating and increasing the risk of a fire.

    Product
    BMW — BMW R 18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3331-2026·2026-10-07

    Penumbra RED 62 Reperfusion Catheter Recalled for Fracture Risk

    Penumbra Inc. is recalling 43 RED 62 Reperfusion Catheters due to manufacturing issues that may cause the catheters to fracture.

    Product
    Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter) Model/Catalog Number: THNDRRED62SKIT Software Version: N/A Product Description: Product common name: Percutaneous catheter A complete product description…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2026·2026-10-07

    Par Health Recalls Buprenorphine Hydrochloride Injection Due to Crystallization

    Par Health USA is voluntarily recalling 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. The FDA classifies this as a Class II recall.

    Product
    BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3294-2026·2026-10-07

    FDA Recalls Medical Kits with Contaminated Pericare Wipes

    American Contract Systems Inc. is recalling 1,804 medical kits containing BD CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.

    Product
    Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL HYSTERECTOMY - 205989 Model No. MHAH55AM LAVH-LAP COLON Model No. SPLL54U VAG HYST PACK Model No. SPVH62P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3302-2026·2026-10-07

    Heraeus Medical Recalls PALACOS R+G pro Bone Cement Due to Leakage Risk

    Heraeus Medical GmbH is recalling PALACOS R+G pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall affects 59,660 units distributed worldwide.

    Product
    PALACOS R+G pro 40; PALACOS R+G pro 80. Model/Catalog Number: 5081288; 5081289. Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3293-2026·2026-10-07

    Recall of Medical Convenience Kits with Contaminated Pericare Wipes

    American Contract Systems Inc. is recalling 1,804 medical convenience kits containing potentially contaminated perineal care wipes. The contamination may cause skin irritation or increase infection risk.

    Product
    Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays CARDIAC HEART BUNDLE NS Model No. LMCH99P OPEN HEART 2 RCH¿ 0248495 Model No. RCOH62C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3324-2026·2026-10-07

    Percussionaire Travel Air and Phasitron 5 Recall for Anesthetic Warning

    Percussionaire Corporation is recalling Travel Air and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.

    Product
    Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3296-2026·2026-10-07

    Cardinal Health Recalls Presource Packs Due to Potential Handpiece Leakage

    Cardinal Health 200, LLC is recalling 344 Presource Packs containing Stryker tube sets because handpieces may leak fluid, creating a slip and fall hazard.

    Product
    Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT,GU DAVINCI , Catalog Number: PGVMDVBWU; 2) KIT,GU DAVINCI , Catalog Number: PGVMDVBWV; 3) KIT,GU DAVINCI , Catalog Number: PGVMDVB26; 4) KIT,GU DAVINCI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3301-2026·2026-10-07

    Heraeus Medical Recalls PALACOS R pro Bone Cement Due to Leakage Risk

    Heraeus Medical is recalling PALACOS R pro 40 and 80 bone cement because of a potential for monomer liquid leakage. The recall affects 33,727 units distributed worldwide.

    Product
    PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).
    Category
    Medical Device
    Distribution
    Distributed nationwide