The Recall Desk

State

Rhode Island product recalls

73,817 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 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 708 (23%) are Severe.

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46101–46125 of 76871

  • ModerateFDA (Drugs)·D-0510-2017·2017-03-15

    LEO Pharma Recalls Calcipotriene Cream Due to Labeling Errors

    LEO Pharma is recalling 272,062 tubes of Calcipotriene Cream because the label omitted a required excipient and a warning about contact dermatitis.

    Product
    CALCIPOTRIENE — CALCIPOTRIENE (CALCIPOTRIENE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1403-2017·2017-03-15

    Merge Cardio software recalled for incorrect measurement units in reports

    Merge Healthcare is recalling Merge Cardio software versions 9.0 and 10.0 because measurements from images or US carts do not transfer to reports in the correct unit of measure.

    Product
    Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1424-2017·2017-03-15

    Siemens Biograph Mobile PET/CT Recall for Missing Instructions

    Siemens is recalling nine Biograph Mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population of devices.

    Product
    Biograph 16 TruePoint - 3R, Material Number 10249555 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1431-2017·2017-03-15

    Merge PACS Software Recalled for Telmed Protocol Data Propagation Failures

    Merge Healthcare is recalling specific versions of Merge PACS software because studies may fail to propagate or import via the telmed protocol.

    Product
    Merge PACS software. The firm name on the label is Merge Healthcare.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1422-2017·2017-03-15

    Siemens Biograph 6 TruePoint PET/CT Recall for Missing Instructions

    Siemens is recalling 18 Biograph 6 TruePoint mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population.

    Product
    Biograph 6 TruePoint, Material Number 10097289 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the purpose of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1425-2017·2017-03-15

    Siemens Biograph Mobile PET/CT Recall for Missing Instructions

    Siemens is recalling four Biograph Mobile PET/CT units because specific mobile instructions were not shipped to a limited population.

    Product
    Biograph 16 TruePoint TrueV - 4R, Material Number 10249556 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2017·2017-03-15

    Sandoz Recalls Pioglitazone and Glimepiride Tablets Due to Dissolution Failure

    Sandoz Inc is recalling specific lots of Pioglitazone and Glimepiride Tablets because they failed to meet dissolution specifications.

    Product
    Pioglitazone and Glimepiride Tablets, USP, 30 mg/4 mg, 30 count bottles, Rx only, Manufactured by Lek Pharmaceuticals d.d., Verovskova Ulica 57, Ljubljana, - SI-1526, Slovenia --- NDC 0781-5635-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1419-2017·2017-03-15

    Siemens Progesterone Test Recalled Due to DHEA-S Interference

    Siemens Healthcare Diagnostics is recalling Dimension Vista LOCI Progesterone tests because DHEA-S causes falsely elevated results.

    Product
    Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vitro diagnostic use in the quantitative determination of progesterone in serum and using the ADVIA Centaur¿, ADVIA Centaur XP, ADVIA Centaur XPT and ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1418-2017·2017-03-15

    Siemens ADVIA Centaur Progesterone Test Recalled for DHEA-S Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Progesterone tests because DHEA-S causes falsely elevated results.

    Product
    ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro diagnostic test for the quantitative measurement of progesterone in human serum and plasma on the Dimension Vista¿System. Progesterone measurements are used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1423-2017·2017-03-15

    Siemens Biograph Mobile PET/CT Recall for Missing Instructions

    Siemens Medical Solutions is recalling six Biograph Mobile PET/CT units because mobile-specific instructions were not shipped to a limited population of systems.

    Product
    Biograph 6 TruePoint, Material Number 10097290 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the purpose of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1410-2017·2017-03-15

    Integra UNI-CP System Recalled for Incorrect Labeling

    Integra LifeSciences Corp. is recalling 39 units of the UNI-CP System due to incorrect labeling on the plate.

    Product
    The UNI-CP System; Model Number: 330230SND.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V174000·2017-03-14

    Navistar Recalls International Trucks Due to Air Dryer Bracket Fracture Risk

    Navistar is recalling 2016-2018 International heavy diesel trucks because a mounting bracket may fracture, causing air leaks and increased stopping distance.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V178000·2017-03-14

    Mercedes-Benz Recalls 2016 G550 and G63 Due to Door Cable Defect

    Mercedes-Benz is recalling 2016 G550 and G63 vehicles because a door cable may break, preventing occupants from opening the door from inside after a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V175000·2017-03-14

    Altec Recalls 2015-2016 Aerial Devices and Service Body Trucks

    Altec is recalling 2015-2016 Aerial Devices and Service Body Trucks due to a wiring defect that may cause a short circuit and increase fire risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V173000·2017-03-14

    Volvo Bus Recalls 2016-2017 9700 Models for Engine Stall Risk

    Volvo Bus is recalling 2016-2017 9700 transit buses because a ground cable may be improperly installed, causing the engine to stall unexpectedly.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V167000·2017-03-14

    Jayco Recalls 2017 Designer Fifth Wheels Due to Spare Tire Rubbing

    Jayco is recalling 2017 Designer fifth wheel trailers because the spare tire rim may rub against the brake caliper, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL DESIGNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17109·2017-03-14

    Energizer XBOX ONE 2X Smart Chargers Recalled Due to Burn Hazard

    Performance Designed Products is recalling Energizer XBOX ONE 2X Smart Chargers because they can overheat and damage controllers, posing a burn risk.

    Product
    Energizer® XBOX ONE 2X Smart Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V171000·2017-03-14

    Forest River Cherokee Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2017 Cherokee recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to installing wrong replacement tires.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V177000·2017-03-14

    Mercedes-Benz Recalls Vehicles Due to Potential Air Bag Deployment Issues

    Mercedes-Benz is recalling various models because incorrect software in control units may prevent air bags from deploying correctly in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C250, C300, C350, CLS550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V176000·2017-03-14

    Mercedes-Benz Recalls 2017 E300 Models for Front Passenger Air Bag Defect

    Mercedes-Benz is recalling 2017 E300 and E300 4Matic vehicles because the front passenger air bag may not deploy properly in certain seating positions, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V160000·2017-03-13

    Spartan Trucks Recalled for Front Suspension Ball Joint Separation Risk

    Spartan Motors is recalling specific 2011-2018 trucks because front suspension ball joints can loosen, potentially causing a loss of steering control.

    Product
    SPARTAN — SPARTAN K4, METROSTAR, K3, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V168000·2017-03-13

    Ford Recalls 2017 Mustangs for Door Handle Spring Defect

    Ford is recalling 2017 Mustangs because the driver-side door handle spring may loosen, allowing the door to unlatch in a crash.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide