The Recall Desk

State

Rhode Island product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57276–57300 of 76887

  • HighFDA (Devices)·Z-1256-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps for RAPIDLyte blood collection devices because they may not attach properly, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 100 uL , Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311053 Legacy Part number: 478601
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1248-2015·2015-03-18

    GE Healthcare Recalls Proteus XR/a X-ray Systems Due to Cable Breakage Risk

    GE Healthcare is recalling Proteus XR/a X-ray systems because a steel cable supporting the bucky device may break. A falling bucky could injure a patient or operator.

    Product
    GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2015·2015-03-18

    Siemens CT System Recalled for Image Artifacts and Safety Issues

    Siemens Medical Solutions is recalling 12 SOMATOM Force CT systems due to potential image artifacts and safety-related software issues.

    Product
    SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 and/or VA50A_SP0; Computed tomography system. Product Usage: The intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1258-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 50/60 uL, Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10328655 Legacy Part number: 478527
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2015·2015-03-18

    Synthes Inserter for Titanium Elastic Nails Recalled for Mechanical Failure

    Synthes, Inc. is recalling Inserter for Titanium Elastic Nails due to potential mechanical failures including shaft breakage and chuck malfunction.

    Product
    Synthes Inserter for Titanium Elastic Nails; The Inserter for Titanium Elastic Nails (TEN) is intended for fixation of diaphyseal fractures where the canal is narrow or flexibility of the implant is paramount. This includes: lower extremity fractures in pediatric and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15E022000·2015-03-18

    Woodstock Stop Arms Recalled for Non-Compliant Border Width

    Woodstock Safety Mirror Co. is recalling specific Stop Arms because the border width is too narrow, reducing visibility and failing federal safety standards.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1261-2015·2015-03-18

    Dako Automated Slide Stainers Recalled for Potential Diagnostic Errors

    Dako North America Inc. is recalling four models of automated slide stainers because a defect may cause buffer leakage, leading to false negative diagnostic results.

    Product
    Autostainer Link 48 (AS480), Autostainer Plus Link Instrument (AS100), Autostainer (S3400), and Autostainer Plus (S3800). Automated slide stainer for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V158000·2015-03-18

    Charles Machine Recalls Ditch Witch T18 Trailers Due to Wheel Lockup Risk

    Charles Machine is recalling 2013-2015 Ditch Witch T18 trailers because incorrect bearing pre-loads may cause wheels to lock up, increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1257-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 140/175 uL, Package count 100 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311054 Legacy Part number: 478605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1262-2015·2015-03-18

    Medela Recalls Sterile Enteral Feeding Syringes Due to Packaging Breach

    Medela Inc. is recalling sterile enteral feeding syringes because a potential packaging breach may have compromised their sterility.

    Product
    - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 60ml Nutrio Enteral Feeding Syringe (sterile) - TL-INT-60 60ml Nutrio Enteral Feeding Syringe with Twistlok adapter (sterile) - INT-60 60mL Nutrio Intopo Enteral Feeding Syringe (sterile) - NGF-60 60ml Nutrio…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1259-2015·2015-03-18

    Arrow Intra-Aortic Balloon Catheter Kit Recalled for Potential Helium Leak

    Arrow International Inc is recalling 166 units of Intra-Aortic Balloon Catheter Kits due to a potential leak that allows helium to escape.

    Product
    Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB), 8 Fr 40 cc Model: IAB-05840-LWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15C001000·2015-03-18

    Graco Recalls Child Seats Due to Missing Instruction Manual Label

    Graco is recalling specific child seats manufactured in 2014-2015 because they lack a label indicating where to find the instruction manual, potentially leading to improper use.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1252-2015·2015-03-18

    Siemens RAPIDPoint 405 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 3,420 RAPIDPoint 405 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 405 Blood Gas Analyzer; Siemens Material Number: 10310464, 10322347, 10314817, 10317193, 10318999, 10320055, 10322347, 10328278, 10328302, 10336784. These systems are intended for near-patient and laboratory testing of blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0408-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling Simvastatin Tablets, 40mg, because the product failed a known impurity specification. The recall affects 13,488 bottles distributed nationwide.

    Product
    Simvastatin Tablets, USP, 40mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-0040-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1265-2015·2015-03-18

    Southern Implants Recalls Dental Implants Due to Labeling Mismatch

    Southern Implants, Inc. is recalling 130 units of MAX-TL and Z-MAX dental implants because the labeled packages contained the wrong implant type.

    Product
    MAX-TL 9.0 x 7.0 mm Implant, Catalog No. 15711K; Z-MAX Implant 9.0 x 7 mm Length, Catalog No. Z-MAX9-7. Dental implant. Product Usage: The MAX Implant is intended to be implanted in the upper and lower jaw arches to provide support for fixed or removable dental prostheses…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0409-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling 13,464 bottles of Simvastatin 80mg tablets because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 80mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-080-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1255-2015·2015-03-18

    Siemens RAPIDLab 1265 System Recalled for Neonatal Bilirubin Variability

    Siemens Healthcare Diagnostics Inc is recalling 2,863 RAPIDLab 1265 Systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1265 System; Siemens Material Number: 10491395, 10321852, 10335524. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2015·2015-03-18

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 4,376 RAPIDPoint 500 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 500 Blood Gas Analyzer; Siemens Material Number: 10492730, 10696855, 10696857, 10697306. The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0411-2015·2015-03-18

    Qualitest Recalls Promethazine DM Syrup Due to Plastic Particulates

    Qualitest Pharmaceuticals is recalling 972 bottles of Promethazine DM Syrup because plastic cap closure particulates may be present in the product.

    Product
    PROMETHAZINE DM SYRUP (Promethazine Hydrochloride, USP and Dextromethorphan Hydrobromide, USP), EACH 5 ml (ONE TEASPOONFUL) CONTAINS: Promethazine Hydrochloride 6.25 mg, Dextromethorphan Hydrobromide 15 mg, alcohol 7%, ONE PINT (574 mL), Rx only, Manufactured for: QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2015·2015-03-18

    Siemens RapidLab 1245 System Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 241 RapidLab 1245 systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1245 System; Siemens Material Number: 10321844, 10491393, 10337179. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1263-2015·2015-03-18

    Ortho-Clinical VITROS Hand-held Barcode Scanner Recall for Sample Skipping

    Ortho-Clinical Diagnostics is recalling VITROS Hand-held Barcode Scanners because they may skip sample cup positions when using the Batch Programming option.

    Product
    VITROS Hand-held Barcode Scanner, Catalog Number 6844210, for use with the following VITROS Systems: VITROS 5,1 FS Chemistry System, VITROS 3600 Immunodiagnostics System, VITROS 4600 Chemistry System, VITROS 5600 Integrated System. This product is an accessory for use with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1408-2015·2015-03-18

    Keystone Food Products Recalls Veggie Sticks and Straws Due to Labeling Error

    Keystone Food Products is recalling specific brands of veggie sticks and straws because the sodium content listed on the label is incorrect.

    Product
    Weis Veggie Sticks Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natures Place Veggie Straws Net Wt. 6 oz Distributed By: DZA Brands, LLC, Salisbury NC 28147/Scarborough, ME 04074 With code dates: 6 Jan 2015…
    Category
    Food
    Distribution
    8 states
  • LowFDA (Drugs)·D-0407-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling specific lots of Simvastatin Tablets, 20mg, because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 20mg a) 90- count bottle (42517-0020-10), b) 1000-count-bottle (NDC 42571-0020-10), Rx only, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc.,Princeton, NJ 08540
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1407-2015·2015-03-18

    Keystone Food Products Recalls Veggie Chips for Incorrect Sodium Labeling

    Keystone Food Products Inc. is recalling specific brands of veggie chips because the sodium content on the label is incorrect. The product contains approximately 290 mg of sodium per serving, not the 55 mg claimed.

    Product
    Weis Veggie Chips Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natures Place Veggie chips Net Wt. 6 oz Distributed By: DZA Brands, LLC, Salisbury NC 28147/Scarborough, ME 04074 With code dates: 15 Dec 2014…
    Category
    Food
    Distribution
    8 states