The Recall Desk

State

Rhode Island product recalls

73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,053
Critical
221
Severe
707
Most recent
2026-10-28

Of the 3,053 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 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38026–38050 of 76794

  • HighFDA (Food)·F-0026-2019·2018-10-17

    Sarap Asian Fusion Recalls Ube Cookies & Cream for Undeclared Allergens

    Sarap Asian Fusion is recalling Ube Cookies & Cream because the product contains undeclared wheat, soy lecithin, and milk.

    Product
    Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product; NET WT. 65 G/Cookie; Contains: Flour, eggs, Baking Soda, Baking Powder, Milk Powder, White Sugar, Brown Sugar, Salt, Butter, Ube, Vanilla extract, cookies & cream chocolate. MFG at 12042 West St. Garden Grove…
    Category
    Food
    Distribution
    44 states
  • HighFDA (Food)·F-0022-2019·2018-10-17

    Whole Foods Recalls 365 Everyday Value White Corn Chips for Undeclared Milk

    Whole Foods Market is recalling 365 Everyday Value White Corn Chips because they may contain undeclared milk. The affected products were distributed nationwide in the US and Canada.

    Product
    365 Everyday Value Brand White Corn Chips, Salted NET WT 20 oz. (1 LB 4 OZ) 567 g packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0080-2019·2018-10-17

    Ortho-Clinical Diagnostics Recalls VITROS 5600 Integrated Systems

    Ortho-Clinical Diagnostics is recalling refurbished VITROS 5600 Integrated Systems because they may dispense insufficient sample volumes without suppressing potentially incorrect results.

    Product
    VITROS 5600 Integrated System- (Refurbished). For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, Catalog Number: 6802915
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0076-2019·2018-10-17

    AngioDynamics BioFlo Port Recall Due to Incorrect Sterile Assembly

    AngioDynamics is recalling BioFlo Ports that were partially manufactured with the wrong sterile port assembly. The devices were distributed in Indiana.

    Product
    BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED PG UPN: H965440210 Catalog Number: 44-021 Box of 1 Port - Product Usage - Long-term access to the central venous system for administration of fluids including but not limited…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2019·2018-10-17

    Pfizer Recalls Glipizide XL Tablets Due to Manufacturing Deviations

    Pfizer is recalling 7,777 bottles of Glipizide XL 5 mg tablets because rejected product was used in manufacturing, violating CGMP standards.

    Product
    Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0077-2019·2018-10-17

    Instrumentation Laboratory Recalls HemosIL ReadiPlasTin Diagnostic Reagent

    Instrumentation Laboratory is recalling 9,751 kits of HemosIL ReadiPlasTin due to potential imprecision and out-of-range quality controls.

    Product
    Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 - Product Usage - HemosIL¿ ReadiPlasTin is an in vitro diagnostic thromboplastin reagent, based on recombinant human tissue factor, for the quantitative determination, in human citrated plasma, of Prothrombin Time (PT)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2019·2018-10-17

    Stryker Spine AVS Aria Cage Recalled for Incorrect Marker Placement

    Stryker Spine is recalling five AVS Aria Cage units because the anterior and posterior markers were placed on the incorrect sides of the device.

    Product
    AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2019·2018-10-17

    Implant Direct Legacy Implant Closed-Tray Transfer Mislabeled Cap Recall

    Implant Direct is recalling 217 units of Legacy Implant Closed-Tray Transfer components due to potential cap mislabeling. The correct part number is on the main vial label.

    Product
    Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile, 3.5mmD Platform. Dental implant component, used temporarily during impressions for the prosthetic procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0095-2019·2018-10-17

    GE Healthcare CARESCAPE Monitor B450 Recalled for Network-Related Restart Issues

    GE Healthcare is recalling CARESCAPE Monitor B450 units because they may restart simultaneously and fail to complete the process if connected to an overloaded network.

    Product
    GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of CARESCAPE B450 in 510(k) countries [UR_CRSCP-885]: The CARESCAPE Monitor B450 is a multi-parameter patient monitor intended for use in multiple areas and intrahospital transport within a professional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0096-2019·2018-10-17

    GE Healthcare CARESCAPE Monitor B850 Recalled for Network-Related Restart Issues

    GE Healthcare is recalling CARESCAPE Monitor B850 units because they may simultaneously restart during prolonged network overload, preventing the restart from completing until the network issue is corrected.

    Product
    GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of CARESCAPE B850 V2 in 510(k) countries [UR_CRSCP-1046]: The CARESCAPE Monitor B850 is a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2019·2018-10-17

    InvaGen Recalls Amlodipine Besylate Tablets Due to Subpotency

    InvaGen Pharmaceuticals is recalling one lot of Amlodipine Besylate 10 mg tablets because the product failed to meet assay specifications at 3-month stability conditions.

    Product
    AMLODIPINE BESYLATE — AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0088-2019·2018-10-17

    GSK Recalls Prevacid 24HR Capsules Due to Manufacturing Deviations

    GSK is voluntarily recalling Prevacid 24HR capsules nationwide due to Current Good Manufacturing Practice (CGMP) deviations. No illnesses have been reported.

    Product
    Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0011-2019·2018-10-17

    Jubilant Cadista Recalls Pantoprazole Tablets Due to Dark Discoloration

    Jubilant Cadista Pharmaceuticals is recalling 158,466 bottles of 40 mg pantoprazole sodium delayed-release tablets due to dark discoloration or brown spots on the edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0016-2019·2018-10-17

    Xiromed Recalls Altavera Tablets Due to Generic Name Mislabeling

    Xiromed LLC is recalling Altavera tablets because the generic name on the packaging may cause confusion. The FDA classifies this as a Class III recall.

    Product
    ALTAVERA — ALTAVERA (LEVONORGESTREL AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0081-2019·2018-10-17

    BD FocalPoint Slide Profiler Recalled for Temperature Limit Labeling Error

    Becton Dickinson is recalling BD FocalPoint Slide Profiler and GS Review Station units because they may not function below 15°C. The agency states this issue has no potential to cause harm.

    Product
    BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station; Catalog Nos. 490398, 490653, 491085, 491086, 491090, 490189 The BD FocalPoint GS Imaging System is intended to assist in cervical cancer screening of BD SurePath Liquid-based Pap Test slides to detect evidence…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V728000·2018-10-16

    Altec Recalls 2015-2017 Aerial Devices Due to Fire Risk

    Altec is recalling 2015-2017 TA45M and AM50/55 aerial devices because a faulty DC-DC converter can cause a fire.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E096000·2018-10-16

    Streetcar Recalls Aftermarket Suspension Kits for RAM Trucks

    Streetcar ORV LLC is recalling aftermarket suspension kits for 2013-2018 RAM 2500 and 3500 trucks because improper installation may weaken the steering connection, increasing crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V729000·2018-10-16

    Grand Design Recalls 2019 Reflection Travel Trailers Due to Wiring Defect

    Grand Design is recalling 2019 Reflection travel trailers because incorrect wiring on the 50-amp mini-breaker may leave the circuit unprotected, increasing fire risk.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V730000·2018-10-16

    Yamaha Recalls SR400 Motorcycles Due to Engine Oil Leak Risk

    Yamaha is recalling 2015-2018 SR400 motorcycles because an engine oil line nut may be loose, causing oil to leak onto the rear tire and increasing crash risk.

    Product
    YAMAHA — YAMAHA SR400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19010·2018-10-16

    Gold Recalls Eddie Bauer Infant Carriers Due to Fall Hazard

    Gold Inc. is recalling Eddie Bauer fabric infant carriers because buckles can break, posing a fall hazard to children. No injuries have been reported.

    Product
    Eddie Bauer fabric infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V723000·2018-10-15

    Keystone Recalls 2019 Fifth Wheels and Travel Trailers for Axle Bearing Defect

    Keystone RV Company is recalling 2019 Dutchmen, Keystone, and Crossroads fifth wheels and travel trailers because axles may be missing inner bearing races, which can cause bearing failure and affect vehicle handling.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS AEROLITE, BULLET, COUGAR, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V722000·2018-10-15

    Forest River Recalls School Buses Due to Seat Foam Impact Defect

    Forest River is recalling certain Starcraft and StarTrans school buses because the seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, STARTRANS QUEST, PRODIGY, SENATOR II, QUEST XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V726000·2018-10-15

    Keystone Recalls 2019 Crossroads Fifth Wheels Due to Awning Switch Defect

    Keystone is recalling 2019 Crossroads Cruiser and Volante fifth wheels because defective awning switches may allow the awning to unroll while the vehicle is moving.

    Product
    CROSSROADS — CROSSROADS VOLANTE, CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide