State

Rhode Island product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10226–10250 of 76142

HighFDA (Devices)·Z-2577-2024·2024-08-21
Merit Medical Catheter Kits Recalled for Syringe Leaks and Breakage Issues
Merit Medical convenience kits containing defective plastic syringes are being recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects approximately 4,027 kits distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced CSG (Introducer Catheter kit), REF: FCL-083-02/A WOR-CSG-B1-09/A WOR-CSG-B2-09/A WOR-CSG-BL1-09/A WOR-CSG-E-90/A For the int
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2573-2024·2024-08-21
Merit Medical Convenience Kits Recalled Due to Defective Syringes
Merit Medical convenience kits containing recalled plastic syringes have quality issues including leaks and breakage that may pose risks during vascular and cardiac procedures. Approximately 5,700 affected kits were distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiography/Angioplasty kit), REF: OPT0242-00 S1279-01 S2953 S2960 S6002 To support various vascular or cardiac diagnostic and interv
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2574-2024·2024-08-21
Merit Medical cardiac kits contain plastic syringes with quality defects
Merit Medical convenience kits used in cardiac procedures contain plastic syringes with potential leaks and breakage. The defects were identified following an FDA Safety Alert issued March 19, 2024.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP (Introducer Catheter kit), REF: For the introduction of various types of pacing leads and catheters to the heart and coronary venous system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2558-2024·2024-08-21
Merit Medical Convenience Kits with Recalled Syringes Pose Quality Risks
Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage that may pose patient safety risks in cardiac and vascular procedures.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiography/angioplasty kit), REF: K12T-10773 K12T-09284D K12T-10621 K12T-10800 K12T-12491 To support various vascular or cardiac dia
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2572-2024·2024-08-21
Merit Medical Convenience Kits with Defective Syringes Recalled
Merit Medical convenience kits containing defective syringes are being recalled for leaks and breakage that may pose a risk to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude Prestige (Introducer Catheter), REF: PLP-2505/A PLP-2514/A PLP-2516/A The introduction of various types of pacing/defibrillator leads and catheters i
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1729-2024·2024-08-21
Pariva Marinated Labneh Bites Recalled Due to Mold Contamination
Pariva LLC is recalling Pariva Marinated Labneh Bites Za'atar (8 oz) due to potential mold contamination. The product was distributed in seven Northeast states with best-by dates in October or December 2024.
Product
Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREAM, SKIM MILK, WHEY PROTEIN CONCENTRATE, SALT AND PECTIN), *SUNFLOWER OIL, *EXTRA VIRGIN OLIVE OIL, SESAME SEEDS, SPICES; CONTAINS: MILK, SESAME; Distributed by,
Category
Food
Distribution
7 states
HighNHTSA·24V624000·2024-08-21
Escape travel trailer cooktop circuit boards may fail and overheat
Escape Trailer is recalling certain 2024 travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat. 248 units are affected.
Product
ESCAPE — ESCAPE ESCAPE 23, ESCAPE 17, ESCAPE 19, ESCAPE 21
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2567-2024·2024-08-21
Convenience kits by Merit Medical recalled for syringe defects
Merit Medical convenience kits containing defective syringes have been recalled nationwide. Identified quality issues including leaks and breakage may pose risks during cardiac and vascular procedures.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K12T/12PI (Custom Pressure Monitoring Kit), REF: K12-03846 K12-04185A K12-03447 K12M-02489 K12-10056 K12-02489A K12-02097B K12-12335 K12-12192P K12-12079
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V627000·2024-08-21
Morbark Recalls 2018-2024 Trailers Due to Electrical Fire Risk
Alamo Group is recalling specific Morbark trailers because loose wires in the power module may cause electrical arcing and fire.
Product
MORBARK — MORBARK EEGER BEEVER 2230, EEGER BEEVER 1821, EEGER BEEVER 2131, M20
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2413-2024·2024-08-21
Dental X-Ray Device Testing Defect May Affect Image Repeatability
Palodex Group Oy recalls the Orthopantomograph OP300 dental x-ray system due to a testing software defect that may allow devices with poor image repeatability to be distributed.
Product
Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2619-2024·2024-08-21
Surgical Lights Recalled for Possible Weld Defect and Frame Detachment
DKK Dai-Ichi Shomei Co., Ltd. is recalling 822 Aurora surgical light heads due to a weld defect that could cause the light head to sag, crack, or detach during use.
Product
Aurora 2 Series, Aurora 7 lighthead; Models: AUR7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0632-2024·2024-08-21
Ophthalmic solution recalled for defective container with lodged spike
FDC Limited recalls Timolol Maleate eye drops (362,544 bottles) nationwide due to a manufacturing defect: a yellow spike from the cap lodged in the nozzle, posing a risk of eye injury.
Product
TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2618-2024·2024-08-21
Aurora 7 Surgical Light Heads Recalled for Cracked Weld Frames
DKK Dai-Ichi Shomei is recalling 555 Aurora 7 surgical light heads because frame welds can crack, causing the frame to sag, the housing to crack, or the light head to detach.
Product
Aurora Series, Aurora 7 lighthead; Models: LED7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1730-2024·2024-08-21
Pariva Marinated Labneh Bites Recalled Due to Potential Mold Contamination
Pariva LLC is recalling Pariva Marinated Labneh Bites Mild Tandoori due to potential mold contamination. Affected products were distributed in Massachusetts, Maine, New Hampshire, Rhode Island, New York, New Jersey, and Connecticut.
Product
Pariva Marinated Labneh Bites Mild Tandoori; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREAM, SKIM MILK, WHEY PROTEIN CONCENTRATE, SALT AND PECTIN), *SUNFLOWER OIL, *EXTRA VIRGIN OLIVE OIL, SPICES; CONTAINS: MILK, Distributed by, Mayur, LLC, 196
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2559-2024·2024-08-21
Merit Medical catheter extractor kits recalled for syringe quality defects
Merit Medical is recalling 3,631 catheter extractor convenience kits due to defective syringes with leaks and breakage. The identified quality issues may compromise patient safety during catheter removal.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Outake, REF CET200 and CET300, The Catheter Extractor is a catheter accessory device intended for minimally invasive removal of tunneled long term catheters. T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2621-2024·2024-08-21
Surgical Lighting Equipment Recalled for Cracked Welds and Frame Detachment Risk
Aurora Series surgical light heads are recalled due to cracked welds on the frame. The defects can cause the frame to sag, housing to crack, or the light head to detach.
Product
Aurora 4 Series, Aurora 7 lighthead; Models: AUA7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2617-2024·2024-08-21
Spinal Cord Stimulation Devices May Reset During Charging, Causing Transient Therapy Loss
Boston Scientific spinal cord stimulation implants may reset during routine charging, causing brief loss of therapy. Patients may experience undesired sensations when stimulation restarts, potentially leading to surgical intervention requests.
Product
WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2566-2024·2024-08-21
Merit Medical Pressure Monitoring Kits with Defective Syringes Recalled
Merit Medical is recalling 69 convenience kits containing defective syringes that may leak or break, potentially risking patient safety during medical procedures. The kits were distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K11 (Custom Pressure Monitoring Kit), REF: K11-00382C To support fluid administration into the body and physiological pressure monitoring. To support various v
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2569-2024·2024-08-21
Merit Medical pericardiocentesis kits recalled for syringe defects
Merit Medical convenience kits containing plastic syringes have been recalled nationwide. The syringes have quality issues including leaks and breakage that may pose a risk to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: PC (Pericardiocentesis Tray - Fluid drainage tray), REF: PC101/B PC801 PC801/A PC802 PC802/A The Pericardiocentesis Kit is intended to withdraw fluid from
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2575-2024·2024-08-21
Merit Medical Cardiac Catheter Kits Recalled for Syringe Leaks and Breakage
Merit Medical's Prelude SNAP-H cardiac catheter kits are being recalled because their syringes may leak or break during use, potentially affecting cardiac procedures. No illnesses have been reported.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP-H (Introducer Catheter kit), REF: PLSH-1006/A PLSH-1007/A PLSH-1008/A PLSH-1009.5/A PLSH-2506/A PLSH-2507/A For the introduction of various t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2565-2024·2024-08-21
Merit Medical Convenience Kits With Recalled Syringes Pose Quality Defect Risks
Merit Medical convenience kits containing recalled syringes are subject to a nationwide recall due to quality defects including leaks and breakage that may pose risks to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K10/K10-PI (Custom Waste Management Kit), REF: K10T-05815 K10T-05816 K10-04722C K10-03591KP K10-05530 K10-04291AP K10-04386CP K10T-05227 K10-05120P K10-0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2576-2024·2024-08-21
Medical paracentesis procedure kits recalled for syringe leaks and breakage
Merit Medical is recalling paracentesis procedure kits nationwide containing syringes with identified leaks and breakage. The defects may pose a risk to patient health during medical procedures.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Safety Paracentesis Procedure Tray (Paracentesis Tray kit), REF: SPPT-100/D SPPT-5F-10/D SPPT-5F-10L/B SPPT-5F-10S SPPT-5F-12PL SPPT-5F-17PL SPPT-5F-7/D SP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2557-2024·2024-08-21
Merit Medical convenience kits recalled for syringe leaks and breakage
Merit Medical convenience kits containing recalled syringes have quality issues including leaks and breakage that may pose a risk to patient health. The recall affects 2,388 kits distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid Response Waste Management System Kit, REF BRC-BAL-INT-SL/B An endoscope and accessories is a device used to provide access, illumination, and allow observ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2560-2024·2024-08-21
Merit Medical Syringes in Convenience Kits Recalled for Leaks and Breakage
Merit Medical convenience kits containing plastic syringes are recalled due to leaks, breakage, and quality defects that may pose a risk to patient health. Approximately 3,647 kits were distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K02 (Custom Syringe Kit), REF: K02-00873A, Inject fluids into, or withdraw fluids from, the body.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2561-2024·2024-08-21
Merit Medical convenience kits recalled for syringe leaks and breakage
Merit Medical is recalling 1,390 convenience kits containing plastic syringes with identified quality issues including leaks and breakage. The kits, distributed nationwide, may pose a risk to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K04 (Custom Syringe Kit), REF:K04-00791A An intravascular administration set is a device used to administer fluids from a container to a patient's vascular syst
Category
Medical Device
Distribution
Distributed nationwide