The Recall Desk

State

Rhode Island product recalls

73,827 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.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52626–52650 of 76881

  • LowFDA (Drugs)·D-0524-2016·2015-12-30

    Oasis Medical Recalls HPMC Visoelastic Due to Potential pH Specification Failure

    Oasis Medical is recalling HPMC Visoelastic syringes because the pH may not meet specifications at expiry. The recall covers 14,852 units distributed nationwide and internationally.

    Product
    HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0503-2016·2015-12-30

    Ameditech iCup DX 11 Panel Recall for Reduced Benzodiazepine Reactivity

    Ameditech is recalling iCup DX 11 Panel tests because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0546-2016·2015-12-30

    Philips Brilliance iCT SP CT System Software Feature Recall

    Philips is recalling 12 Brilliance iCT SP CT systems because the perfusion scan feature may be unavailable on specific software versions.

    Product
    Brilliance iCT SP Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0540-2016·2015-12-30

    Ameditech RealityCHECK Tilt Cup Benzodiazepine Test Recall

    Ameditech is recalling 80 kits of RealityCHECK Tilt Cup 12 Panel + Adult tests due to reduced reactivity for two benzodiazepine compounds.

    Product
    RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0487-2016·2015-12-30

    Ameditech 11 Panel Card Recalled for Reduced Benzodiazepine Reactivity

    Ameditech is recalling 50 kits of the 11 Panel Card (OPI 300) w/Adult because the tests showed reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    11 Panel Card (OPI 300) w/Adult, Item No. 71125AA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0519-2016·2015-12-30

    Ameditech ProScreen 10 Panel Dip Card Recall for Reduced Benzodiazepine Reactivity

    Ameditech is recalling ProScreen 10 Panel Dip Cards because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, PSDA-10PPX, PSDA-10BUP, PSD-12BUP, PSD-10M, PSCupA-6MB-W, PSCup-10MMO300, PSD-5AB, PSD-10CMO3, PSCupA-10MO, PSCupA-12M-W I-DXA-1127-023, PSCupA-12TBU.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0501-2016·2015-12-30

    Ameditech Benzodiazepine Drug Test Recall for Reduced Reactivity

    Ameditech is recalling EDI BZO Uncut Sheet drug tests because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    EDI BZO Uncut Sheet - Cup*, Item No. 160170
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0523-2016·2015-12-30

    Oasis Medical Recalls HPMC Visoelastic Topical Due to pH Specification Failure

    Oasis Medical, Inc. is recalling HPMC Visoelastic Topical products because the pH may not meet specifications at expiry.

    Product
    HPMC Visoelastic Topical, 8,000 cps, Reference 5200, 1.5 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0457-2016·2015-12-30

    BC Group International Recalls Defibrillator and Pacer Analyzer Units

    BC Group International is recalling five DA-2006P Defibrillator / Pacer Analyzer units because reversed wires cause inverted waveforms.

    Product
    DA-2006P - Defibrillator / Pacer Analyzer; Product Usage: Intended to measure the output of a defibrillator or transcutaneous pacemaker.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V883000·2015-12-29

    Micro Bird Recalls 2014-2016 School Buses for Loose Wheel Bolts

    Micro Bird is recalling 464 school buses because a camber caster kit bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V884000·2015-12-29

    Micro Bird Recalls Transit Buses Due to Loose Wheel Bolt

    Micro Bird is recalling 2014-2016 G5 and MB II transit buses because a wheel bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V881000·2015-12-28

    Ferrari Recalls 2016 488 GTB Vehicles for Fuel Line Fire Risk

    Ferrari is recalling 119 model year 2016 488 GTB vehicles because a fuel line connection may leak vapor, increasing fire risk.

    Product
    FERRARI — FERRARI 488 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V880000·2015-12-28

    Tiffin Motorhomes Recall 2007-2015 Models Due to Unstable Entry Steps

    Tiffin is recalling 2007-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    TIFFIN — TIFFIN BUS, PHAETON, BAY, ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0417-2016·2015-12-23

    Ashdon Farms Honey Mustard Mix Recalled for Missing Milk Allergen Labeling

    A. L. Schutzman Company, Inc. is recalling Ashdon Farms Honey Mustard Mix because the packaging lists whey but fails to declare milk in the 'Contains' statement.

    Product
    Honey Mustard Mix sold under the following brand: Ashdon Farms, Net Wt. 8 oz. (227 g), UPC 79113-41184
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0297-2016·2015-12-23

    Whole Foods Recalls Classic Deli Pasta Salad Due to Listeria

    Whole Foods Market is recalling Classic Deli Pasta Salad because it is contaminated with Listeria monocytogenes. The product was sold in the Northeast.

    Product
    Classic Deli Pasta Salad, 6oz UPC 0 36406 30001 7
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-0290-2016·2015-12-23

    Whole Foods Recalls Curry Chicken Salad Wrap Due to Listeria

    Whole Foods Market is recalling Curry Chicken Salad Wraps in the Northeast due to Listeria monocytogenes contamination.

    Product
    Curry Chicken Salad Wrap, Made Right Here, sold by weight, 12oz UPC 263144 UPC Code : 285551
    Category
    Food
    Distribution
    7 states