State

Rhode Island product recalls

73,106 recalls have nationwide distribution and so reach Rhode Island. 3,046 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,046
Critical: 221
Severe: 572
Most recent: 2026-09-23

Of the 3,046 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 572 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,046 recalls whose distribution notice names Rhode Island specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11651–11675 of 76152

SevereFDA (Drugs)·D-0486-2024·2024-05-15
Sapropterin Dihydrochloride Powder for Oral Solution Recalled Due to Sub-Potency
Dr. Reddy's Laboratories is recalling 2,402 cartons of Sapropterin Dihydrochloride Powder 100mg due to sub-potency associated with powder discoloration. The affected lot (T2200352) was distributed nationwide.
Product
Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-477-30.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V340000·2024-05-15
2025 MINI Countryman Rear Armrest May Detach During Airbag Deployment
BMW is recalling 9 2025 MINI Countryman vehicles because the armrest support bracket on the rear side door panel may be improperly secured and detach during an airbag deployment, potentially striking occupants or interfering with airbag function.
Product
MINI — MINI COUNTRYMAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0489-2024·2024-05-15
TraMADol HCl 50 mg Tablets Recalled for Foreign Baclofen Tablets
RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.
Product
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0493-2024·2024-05-15
Prescription antifungal injection product recalled for out-of-specification assay
Sun Pharmaceutical is recalling Amphotericin B for Injection (50 mg vials) due to out-of-specification assay results. The recall affects 11,016 vials with lot numbers BAE0055A, BAE0056A, and BAE0068A distributed nationwide.
Product
AMPHOTERICIN B — AMPHOTERICIN B (AMPHOTERICIN B)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2024·2024-05-15
GE Allia IGS Fluoroscopic X-Ray Systems Adhesive Bolt Defect
GE Healthcare recalled certain Allia IGS and related fluoroscopic x-ray systems due to potential incomplete adhesive on bolts in the gantry assembly, risking detector or tube failure.
Product
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2024·2024-05-15
GE Healthcare Allia IGS Fluoroscopic Systems Recall: Missing Adhesive
GE Healthcare recalls Allia IGS and related interventional fluoroscopic x-ray systems due to potentially missing adhesive on bolts. The defect could allow the detector/elevator or x-ray tube in the gantry assembly to fall.
Product
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1757-2024·2024-05-15
Philips 5000 Compact Series Ultrasound Systems pose uncontrolled burn risk
Philips 5000 Compact Series ultrasound systems may leave unselected transesophageal transducers powered without temperature monitoring, risking patient burns during imaging procedures.
Product
5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and Product/REF: 5300 W/795146, 5300 P/795147, 5300 G/795148, used with Deluxe and Premium Carts that come with multiport adapters.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V344000·2024-05-15
2021-2023 Volkswagen ID.4 display software defect increases crash risk
Certain 2021-2023 Volkswagen ID.4 vehicles experience a software issue causing display failures that hide the speedometer and rearview camera. Dealers will update the software at no cost.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2024·2024-05-15
GE Innova IGS Fluoroscopic X-Ray Systems Adhesive Defect Recall
GE Healthcare is recalling certain Innova IGS x-ray systems due to potential adhesive defects on component bolts. Missing adhesive could cause the detector or x-ray tube to fall during use.
Product
GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2024·2024-05-15
Interact Discovery RT X-ray Systems Recalled for Component Fall Risk
GE Healthcare is recalling certain x-ray systems because adhesive material may not be properly attached to bolts, which could cause components to fall during use.
Product
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1784-2024·2024-05-15
X-ray C-arm Tabletop Recalled for Risk of Uncontrolled Motion
NRT X-RAY A/S recalls Intelli-C X-ray tabletops due to faulty firmware and worn motor components that may cause uncontrolled C-arm motion, potentially striking patients or operators.
Product
Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0487-2024·2024-05-15
Tramadol Hydrochloride Tablets Recalled Due to Baclofen Contamination
Advagen Pharma is recalling Tramadol Hydrochloride Tablets after a pharmacy discovered baclofen tablets mixed in a bottle of tramadol. This nationwide recall affects 2,592 bottles.
Product
TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V339000·2024-05-15
Multiple travel trailers recalled for detaching freshwater tanks
Forest River travel trailers may have freshwater tanks that detach when full, posing a road hazard. Dealers will install additional attachment straps at no cost.
Product
VIKING TOWABLE — VIKING TOWABLE, CLIPPER TOWABLE, INDEPENDENCE TRAIL TRAILE VWT182DBU, VWT262BHS, VWT26SBHSAGA, VWT272RLS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0484-2024·2024-05-15
Prescription Duloxetine 60 mg capsules recalled for N-nitroso impurity
Breckenridge Pharmaceutical is recalling Duloxetine 60 mg capsules due to elevated levels of N-nitroso-duloxetine, a manufacturing impurity above FDA limits. No illnesses have been reported.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2024·2024-05-15
GE Healthcare X-Ray Systems Recalled for Loose Bolts on Gantry Assembly
GE Healthcare is recalling x-ray imaging systems because adhesive on critical bolts may not have been applied, potentially causing the detector or x-ray tube to fall. The recall affects 21 units worldwide.
Product
GE Healthcare Innova IGS 5, computed tomography x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0483-2024·2024-05-15
Duloxetine delayed-release capsules recalled for manufacturing impurity exceeding limits
Breckenridge Pharmaceutical recalls Duloxetine 20 mg capsules nationwide after detecting N-nitroso-duloxetine impurity above FDA-recommended limits in approximately 7,188 units from lot 220456, expiring February 2025.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0482-2024·2024-05-15
Duloxetine prescription capsules recalled for N-nitroso impurity exceeding FDA limits
Breckenridge Pharmaceutical recalls Duloxetine 30mg delayed-release capsules nationwide due to N-nitroso-duloxetine impurity exceeding FDA-recommended interim limits. The impurity was identified as a CGMP manufacturing deviation.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1782-2024·2024-05-15
GE Healthcare X-ray Systems: Potential Adhesive Failure Poses Fall Hazard
GE Healthcare is recalling certain Allia and Discovery IGS x-ray systems due to potential adhesive failure that could cause the detector, elevator, or x-ray tube to fall. No injuries reported.
Product
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2024·2024-05-15
GE Healthcare Allia IGS 7 X-ray Systems Adhesive Bolt Failure Recall
GE Healthcare is recalling Allia IGS 7 interventional x-ray systems due to potential adhesive failure on bolts securing the detector and x-ray tube, which could fall during use.
Product
GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1775-2024·2024-05-15
Baxter Spectrum IQ Infusion Pump recalled due to improper pre-release testing
Baxter Healthcare is recalling one Spectrum IQ Infusion Pump that underwent improper testing before release. The device was distributed nationwide including in Massachusetts.
Product
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1759-2024·2024-05-15
Randox Clinical Chemistry Calibration Serum Recalled for Measurement Bias
Randox Laboratories has recalled Clinical Chemistry Calibration Serum (Cal2351/Cal10388) due to negative bias in inorganic phosphate measurements on RX Series instruments. The issue could affect the accuracy of clinical chemistry test results.
Product
Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based serum covering 38 commonly used clinical chemistry tests.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2024·2024-05-15
Spinal Fusion Device Recall: Setscrew Insertion and Tightening Issues
SPINEART's PERLA TL 25D spinal fusion screws are being recalled due to difficulties with setscrew insertion inside the screw head. The setscrew may not be properly tightened or may be positioned incorrectly, potentially affecting spinal stability.
Product
PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S TLF-DS 55 35-S TLF-DS 55 40-S TLF-DS 55 45-S TLF-DS 65 35-S TLF-DS 65 40-S TLF-DS 65 45-S TLF-DS 65 50-S The PERLA¿ TL system is intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1786-2024·2024-05-15
Evidence MultiSTAT analyzer foam gasket malfunction may affect test accuracy
Randox Laboratories is recalling 40 units of the Evidence MultiSTAT analyzer because a foam gasket defect may allow light to leak into the camera during testing, potentially affecting result accuracy and delaying reporting.
Product
Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of parent drug molecule and metabolites of drugs in human urine Catalog Number: EV4115
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2024·2024-05-15
Prescription skin cleanser recalled nationwide due to subpotency
Acella Pharmaceuticals recalled 7,104 bottles of Sodium Sulfacetamide 10% Sulfur 5% Cleanser nationwide because the product contained less active ingredient than labeled. The recall was terminated in December 2025.
Product
SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER — SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER (SULFACETAMIDE SODIUM AND SULFUR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1785-2024·2024-05-15
Stryker Dynamic Mesh Mislabeled with Incorrect Catalog Number
Stryker shipped 63 units of cranial mesh labeled as catalog 56-90614 (Gold) but actually containing 56-90314 (Blue) mesh. The mislabeling may cause procedural delays.
Product
Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614
Category
Medical Device
Distribution
Distributed nationwide