The Recall Desk

State

Rhode Island product recalls

72,940 recalls have nationwide distribution and so reach Rhode Island. 3,043 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,043
Critical
221
Severe
570
Most recent
2026-09-09

Of the 3,043 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 570 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,043 recalls whose distribution notice names Rhode Island specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3651–3675 of 75983

  • ModerateFDA (Devices)·Z-1089-2026·2026-01-21

    Hysterectomy procedure kits recalled over leaking suction irrigators inside

    Medline is recalling 1457 units of procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVINCI HYSTERECTOMY CDS, REF CDS985344F; 4) LAVH, REF DYNJQ9041R; 5) LAPAROSCOPIC HYSTERECTOMY, REF DYNJ900244I; 6) ROBOTIC LAVH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1072-2026·2026-01-21

    Allura Xper FD20 OR Table recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20 OR Table, model 722023, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20 OR Table; Model Number: 722023;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1077-2026·2026-01-21

    Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20/20; Model Number: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1056-2026·2026-01-21

    IV start kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1088-2026·2026-01-21

    Robotic and gynaecology kits recalled over leaking suction irrigators inside

    Medline is recalling 12,584 procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2026·2026-01-21

    Neurostimulator clinician programmer app recalled over faults during device use

    Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.

    Product
    A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1064-2026·2026-01-21

    Allura Xper FD10, model 722003, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10; Model Number: 722003;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1074-2026·2026-01-21

    Allura Xper FD10/10 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 22 units of the Allura Xper FD10/10, model 722027, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10/10; Model Number: 722027;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1076-2026·2026-01-21

    Preoperative kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 11173 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Allura Xper FD20/10; Model Number: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1069-2026·2026-01-21

    Allura Xper FD10/10, model 722011, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 21 units of the Allura Xper FD10/10, model 722011, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10/10; Model Number: 722011;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1060-2026·2026-01-21

    Allura Xper FD10 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 56 units of the Allura Xper FD10, model 722010, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1065-2026·2026-01-21

    Allura Xper FD10/10, model 722005, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10/10; Model Number: 722005;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1085-2026·2026-01-21

    Robotic thoracic and cardiac kits recalled over leaking suction irrigators

    Medline is recalling 96 units of procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1049-2026·2026-01-21

    Allura Xper FD20/10 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20/10, model 722029, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0274-2026·2026-01-21

    Admission and admin kits recalled over recalled B. Braun administration sets

    Medline is recalling 1725 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1053-2026·2026-01-21

    Donor nephrectomy accessory kits recalled over recalled B. Braun sets

    Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1040-2026·2026-01-21

    CT pendant replacement kits recalled for missing a safe hand position label

    Mobius Imaging is recalling 101 detachable 10in pendant replacement components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.

    Product
    Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1041-2026·2026-01-21

    CT pendant upgrades recalled for missing a safe hand position label

    Mobius Imaging is recalling 26 detachable 10in pendant upgrade components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.

    Product
    Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1048-2026·2026-01-21

    Infusion system software recalled to emphasize instructions in the manual

    Fresenius Kabi is recalling 30 units of Ivenix Infusion System LVP software to emphasize the instructions for LVP duration programming set out in the IFU.

    Product
    Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V023000·2026-01-20

    2025 Nissan Sentra door strikers may fail while vehicle in motion

    Nissan is recalling certain 2025 Sentra vehicles because door strikers may have been improperly welded and could break, allowing doors to open while the vehicle is moving. This increases the risk of injury or crash.

    Product
    NISSAN — NISSAN SENTRA, ALTIMA, KICKS, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C001000·2026-01-20

    Evenflo Recalls Titan 65 Child Seats Missing Tether Straps

    Evenflo is recalling specific Titan 65 child seats that may lack a tether strap, which could reduce crash protection and increase injury risk.

    Product
    CHILD SEAT:TETHER: STRAP/WEBBING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V020000·2026-01-19

    Fifth wheel trailer ramp door may break away from its frame

    Forest River is recalling certain fifth wheel travel trailers across the Work and Play, Coachmen Adrenaline, Chaparral, Riverstone, Takoda, Shasta Phoenix and Cedar Creek ranges because the ramp door may break away.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, SHASTA CEDAR CREEK, CHAPARRAL, RIVERSTONE, ADRENALINE
    Category
    Vehicle
    Distribution
    Distributed nationwide