State

Rhode Island product recalls

73,509 recalls have nationwide distribution and so reach Rhode Island. 3,047 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,047
Critical: 221
Severe: 707
Most recent: 2026-10-14

Of the 3,047 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 3,047 recalls whose distribution notice names Rhode Island specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23151–23175 of 76556

HighFDA (Devices)·Z-0442-2022·2022-01-05
Karl Storz Endoscope Sterilization Trays Instructions for Use Updated
Karl Storz Udel Sterilization Tray instructions for use have been updated to correct sterilization methods and clarify endoscope compatibility. Ethylene oxide is now excluded as a sterilization modality.
Product
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD, INLINE CAMERA HEADS); 39301AS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES 4MM X 18CM); 39301BCTS/CAMERA TRAY (INLINE/C-MOUNT CAMERA HEADS); 39301BS/RIGID…
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-0420-2022·2022-01-05
Ultimum Hemostasis Introducer devices recalled due to manufacturing error
Abbott is recalling one lot of Ultimum Hemostasis Introducer devices due to a manufacturing error that resulted in incorrect hub and length. Affected devices are 12 cm long instead of the intended 5 cm.
Product
Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0324-2022·2022-01-05
SterRx Phenylephrine HCl Injection Recalled for Sterility Assurance Failure
SterRx is recalling phenylephrine HCl injectable solution nationwide due to lack of assurance of sterility. The affected product is a 50 mg per 250 mL injection in 0.9% sodium chloride.
Product
PHENYLephrine HCl, 50 mg per 250 mL, (200 mg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-901-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0437-2022·2022-01-05
VIDAS Lyme diagnostic test device recalled due to substrate error
bioMerieux recalled VIDAS Lyme IgG II test devices (two lots) due to a substrate error that prevents tests from running. Users must retest patients, potentially delaying Lyme disease diagnosis.
Product
VIDAS Lyme IgG II (LYM), REF 417401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0423-2022·2022-01-05
Speech Generation Device Charging Components Recalled for Fire and Electric Shock Hazard
Forbes Rehab Services is recalling Monoprice charging cables and iClever charging bricks for ProSlate Speech Generation Devices due to fire and electric shock risks if cables are damaged or charging occurs near moisture.
Product
Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging brick components for the SoundPOD Bluetooth Speaker accessory to the ProSlate Speech Generation Devices (including Proslate 13: B398PS130; Proslate 10: B398PS100…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2022·2022-01-05
VIDAS Mumps IgG diagnostic test kit recalled due to substrate error
bioMerieux is recalling one lot of VIDAS Mumps IgG diagnostic tests because a substrate error prevents the tests from running, causing delays.
Product
VIDAS Mumps IgG (MPG), REF 30218
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2022·2022-01-05
VIDAS procalcitonin diagnostic test substrate error causes testing delays
Nationwide recall of VIDAS procalcitonin test kits for substrate defects that prevent testing and require retesting, potentially delaying diagnostic results.
Product
VIDAS B.R.A.H.M.S. PROCALCITONIN PCT, REF 30450-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2022·2022-01-05
VIDAS Estradiol II Test Device Recalled Due to Substrate Error
bioMerieux is recalling one lot of VIDAS Estradiol II diagnostic test devices due to a substrate error that prevents tests from running, causing delayed results and requiring repeat testing.
Product
VIDAS Estradiol II, REF 30431-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2022·2022-01-05
VIDAS SARS-COV-2 Diagnostic Test Recalled for Substrate Error
bioMerieux is recalling two lots of VIDAS SARS-COV-2 IgG diagnostic tests due to substrate errors that prevent test execution, requiring users to repeat testing and potentially delaying results.
Product
VIDAS SARS-COV-2 IgG, Ref 423834-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2022·2022-01-05
VIDAS Measles IgG Test Kit Recalled Due to Substrate Error
bioMerieux is recalling VIDAS Measles IgG test kits due to a substrate error that prevents the test from running, requiring users to repeat testing and potentially delaying results.
Product
VIDAS Measles IgG (MSG), REF 30219
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22044·2022-01-05
Native Creation Small Wool Sweaters Recalled for Lead Paint on Zipper
Native Creation is recalling approximately 170 small wool sweaters for children sizes 0 to 8 because the zipper pull contains lead paint that exceeds federal limits and poses a toxic ingestion risk to young children.
Product
Native Creation Small Wool Sweaters
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0296-2022·2022-01-05
Lidocaine Hydrochloride Topical Solution Recalled for Superpotency
Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution USP 4% due to superpotency. The affected lot was distributed nationwide.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0433-2022·2022-01-05
VIDAS LH diagnostic test substrate error causes delayed results
bioMerieux VIDAS LH test kits (lot 1008848600) are affected by a substrate error that prevents test execution, requiring users to repeat testing and potentially delaying results.
Product
VIDAS LH, REF 30406-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0431-2022·2022-01-05
Diagnostic test kit recalled due to substrate error preventing test execution
A diagnostic test kit manufactured by bioMerieux has been recalled because a substrate error prevents the test from running, which delays test results for patients.
Product
VIDAS TOXO IgG Avidity (TXGA), REF 30222-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0427-2022·2022-01-05
Diagnostic substrate error in medical testing device causes test failures
bioMerieux is recalling 1,579 VIDAS DEX@ diagnostic devices due to substrate errors that prevent test execution, requiring users to rerun tests and potentially delaying results.
Product
VIDAS DEX@, Dimer Exclusion II, REF 30455-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0422-2022·2022-01-05
Diagnostic device recall: incorrect color in package insert reading table
Biomerieux is recalling RAPID 20 E diagnostic systems because the package insert contains an incorrect color for interpreting negative CIT test results.
Product
RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0438-2022·2022-01-05
VIDAS SARS-CoV-2 IgM Diagnostic Test Recalled for Substrate Error
bioMerieux is recalling one lot of VIDAS SARS-CoV-2 IgM tests nationwide due to a substrate defect that prevents the test from running. The defect causes delayed results as users must repeat testing.
Product
VIDAS SARS-COV-2 IgM, Ref 423833-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0297-2022·2022-01-05
Betamethasone Dipropionate Lotion recalled for failed stability test
Teligent Pharma is recalling Betamethasone Dipropionate Lotion USP 0.05% (Augmented) due to failure to meet specification for the Active Pharmaceutical Ingredient particle test during routine stability testing.
Product
Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0434-2022·2022-01-05
Medical Device FSH Test Substrate Error Causes Failed Tests and Delayed Results
bioMerieux is recalling VIDAS FSH test kits due to substrate errors that prevent the test from running, requiring repeated testing and delaying results.
Product
VIDAS FSH, REF 30407-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0436-2022·2022-01-05
VIDAS Lyme IgM II Diagnostic Test Kits Recalled for Substrate Error
bioMerieux is recalling three lots of VIDAS Lyme IgM II diagnostic test kits due to a substrate error that prevents the test from running, requiring users to conduct another test to obtain results.
Product
VIDAS Lyme IgM II (LYM), REF 416436
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0432-2022·2022-01-05
VIDAS RUB IgG Diagnostic Test Kit Recalled for Substrate Defect
bioMerieux is recalling three lots of VIDAS RUB IgG test kits due to substrate errors that prevent the test from running, potentially delaying diagnostic results.
Product
VIDAS RUB IgG (RBG), REF 30226
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0424-2022·2022-01-05
FDA Recalls VIDAS PRG Progesterone Test Kits for Substrate Error
bioMerieux is recalling 1,818 units of VIDAS PRG Progesterone test kits due to a substrate error that prevents the tests from running properly, causing delayed results when patients need repeat testing.
Product
VIDAS PRG Progesterone, REF 30409-01
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V002000·2022-01-04
LGS Industries Recalls 2014-2021 Trailers with Electric Rear Door Winch Defect
LGS Industries is recalling 2014-2021 trailers because the electric rear door winch cable may break, allowing the door to fall open and increasing injury risk.
Product
LGS INDUSTRIES — LGS INDUSTRIES PREMIER RACE, SHADOW, CARGO SPORT, JOURNEY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V001000·2022-01-01
Rosenbauer Fire Trucks Recalled for Fuel Tube Cracking and Fire Risk
Rosenbauer America is recalling 2018-2022 fire trucks because fuel tubes may crack, causing high-pressure leaks that could lead to fire.
Product
ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, COMMERCIAL 114SD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0288-2022·2021-12-29
Moxifloxacin 1 mg/mL Solution Label Mix-up Recall
Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.
Product
Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42
Category
Drug
Distribution
Distributed nationwide