The Recall Desk

State

Rhode Island product recalls

73,570 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,048
Critical
221
Severe
707
Most recent
2026-10-21

Of the 3,048 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 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25126–25150 of 76618

  • HighFDA (Devices)·Z-2030-2021·2021-07-14

    FREELITE Kappa Free Kit quality control bias recall

    The Binding Site Group is recalling the FREELITE Human Kappa Free Kit due to quality control bias of approximately 10% compared to assigned values. Specific lot numbers distributed worldwide are affected.

    Product
    FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas c Systems, REF: LK016.CB, IVD CE, UDI: 05051700012096
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2026-2021·2021-07-14

    Siemens Atellica Analyzer Valves Recalled for Manufacturing Defect Risk

    Siemens Healthcare Diagnostics has recalled Atellica CH 930 Analyzer valves that may malfunction due to a manufacturing defect. The affected valves may wear and leak over time, potentially impacting diagnostic test accuracy.

    Product
    Atellica CH 930 Analyzer - multi-component system for in vitro diagnostic testing of clinical specimens SMN 11067000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2007-2021·2021-07-14

    Verigene Gram-Positive Blood Culture Test Recalled for Potential False-Negative Results

    Luminex Corporation is recalling the Verigene BC-GP blood culture test (Model 20-006-018) due to the potential for false-negative results. Approximately 36,416 units have been distributed worldwide.

    Product
    Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) Model Number: 20-006-018
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2006-2021·2021-07-14

    Luminex Verigene Respiratory Pathogens Test Recalled for False-Negative Risk

    Luminex Corporation is recalling 38,990 Verigene Respiratory Pathogens Flex nucleic acid tests due to potential false-negative results. The tests were distributed worldwide, including throughout the United States.

    Product
    Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2036-2021·2021-07-14

    Cesarean Birth Drapes recalled due to defective plastic film causing sticking

    Cardinal Health is recalling Cesarean Birth Drapes due to a plastic film defect. The defect causes the drapes to stick, preventing proper unfolding and application during surgery.

    Product
    Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2033-2021·2021-07-14

    Sterile Angiography Drapes Recalled Due to Sticking Plastic Film Defect

    Cardinal Health is recalling 3,192 units of Sterile Radial/Femoral Angiography Drapes due to sticking plastic film that may prevent proper unfolding and application during surgical procedures.

    Product
    Sterile Radial/Femoral Angiography Drape, Catalog Number 29529 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2028-2021·2021-07-14

    Atellica analyzer valves recalled for manufacturing defect affecting diagnostic accuracy

    Siemens recalls Atellica analyzers (CH 930, IM 1300, IM 1600) due to valve manufacturing defects that may cause leaking and affect clinical test result accuracy.

    Product
    Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic testing of clinical specimens SMN 11066000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2013-2021·2021-07-14

    Randox RX Imola Analyzer Software Freeze Recall - 50 Units Affected

    Randox recalls 50 RX Imola Analyser units nationwide and in Puerto Rico due to software freezing that prevents test results from displaying.

    Product
    Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2032-2021·2021-07-14

    Nonsterile Femoral Angiography Drapes Recalled Due to Sticking Plastic Film Defect

    Cardinal Health is recalling 26,250 units of Nonsterile Femoral Angiography Drapes due to a manufacturing defect causing the drapes to stick and preventing proper application. This may compromise surgical site protection.

    Product
    Nonsterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2038-2021·2021-07-14

    Angiography and Cesarean Birth Drapes recalled due to sticking defect

    Cardinal Health is recalling Nonsterile Femoral Angiography and Cesarean Birth Drapes (15,360 units) because plastic film causes sticking that may prevent proper unfolding and application.

    Product
    Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0651-2021·2021-07-14

    Xylocaine Lidocaine Injection Recalled for Low Epinephrine Assay Results

    Fresenius Kabi USA LLC is recalling Xylocaine-MPF with Epinephrine 1:200,000 injection vials nationwide due to low out-of-specification results for epinephrine assay.

    Product
    XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·21163·2021-07-14

    Academy Sports Ozone 500 24-Inch Bicycles Recalled for Fall Hazard

    Academy Sports + Outdoors is recalling about 3,860 Ozone 500 Girls' and Boys' Elevate 24-Inch Bicycles because the rear shock spring can become stuck, creating a pinch point and posing a fall hazard to riders.

    Product
    Ozone 500® Girls' and Boys' Elevate 24-Inch Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2031-2021·2021-07-14

    Sterile Femoral Angiography Drape Sticks; Cannot Unfold Properly

    Cardinal Health is recalling 574 units of Sterile Femoral Angiography Drapes because the plastic film causes the drapes to stick, preventing proper unfolding and application during surgery.

    Product
    Sterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0650-2021·2021-07-14

    Genentech Xolair Injection Recalled for Failed Stability Specifications

    Genentech is recalling two lots of Xolair (omalizumab) injection nationwide due to out-of-specification Polysorbate 20 content detected at the 12-month stability testing timepoint. The affected lots are 3352758 and 3352759, both with August 2021 expiration dates.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0786-2021·2021-07-14

    Hatch Verde Salsa Recalled for Potential Foreign Material

    Heritage Family Specialty Foods, Inc. is recalling Hatch Verde Salsa Medium (12 oz jars) due to potential foreign material contamination. The recall affects 646 cases distributed nationwide.

    Product
    Hatch Verde Salsa Medium Net Wt. 12 oz (340g) 6 jars per case packaged in clamshell container UPC Code: 810041591999
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0787-2021·2021-07-14

    Taco Casa Green Salsa Recalled for Potential Foreign Material

    Heritage Family Specialty Foods is recalling Taco Casa Green Salsa due to potential foreign material contamination. The affected product was distributed nationwide.

    Product
    E6164J2 Taco Casa Green Salsa 8 x 4 lb (1.8 kg) pouches
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateCPSC·21164·2021-07-14

    Walgreens Recalls Disney Baby Winnie the Pooh Rattle Sets for Choking Hazard

    Walgreens is recalling about 54,000 Disney Baby Winnie the Pooh Rattle Sets because the feet can detach and pose a choking hazard to young children. Consumers should immediately remove the rattle from children and contact Walgreens for a refund.

    Product
    Disney Baby Winnie the Pooh Rattle Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2021·2021-07-14

    ACE Control Set stability claim failure requires updated handling instructions

    Sentinel CH SpA is recalling ACE Control Set diagnostic control kits due to stability claims after reconstitution that do not meet specified requirements. Updated handling instructions have been provided to affected users.

    Product
    ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V529000·2021-07-13

    Entegra and Jayco recreational vehicles recalled for window adhesive failure

    Jayco is recalling certain 2019-2021 recreational vehicles with Hehr 6400 series windows due to adhesive failure. The window vent may detach, increasing the risk of crash or injury.

    Product
    ENTEGRA — ENTEGRA, JAYCO ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E063000·2021-07-13

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Leak Risk

    Cummins is recalling specific L9 Diesel Engines equipped with remote Stage 2 fuel filters because a fuel leak may occur from the hose between the fuel pump and filter head.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V530000·2021-07-13

    Micro Bird Recalls School Buses Due to Emergency Door Defect

    Micro Bird is recalling 2003-2022 school buses because the service door emergency release handle may bind, preventing evacuation in an emergency.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, MB II SCHOOL BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V531000·2021-07-13

    Micro Bird Transit Buses Recalled for Service Door Emergency Release Defect

    Micro Bird is recalling 1,323 transit buses because the service door emergency release handle may bind, preventing evacuation in an emergency.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS, T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V526000·2021-07-12

    Mercedes-Benz Recalls 2020 GLB 250 for Electrical Fire Risk

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because an incorrect voltage converter socket may cause excessive voltage in the second-row power outlet, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide