State

Rhode Island product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40701–40725 of 76860

HighFDA (Devices)·Z-1103-2018·2018-03-28
Boston Scientific Recalls Re-Entry Malecot Nephrostomy Catheter Sets
Boston Scientific is recalling specific Re-Entry Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.
Product
Re-Entry" Malecot Nephrostomy Catheter Set, Product Number: M0064101050, GTIN: 08714729192268 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1134-2018·2018-03-28
Medfusion Syringe Pumps Recalled for Syringe Misidentification Risk
Smiths Medical ASD Inc. is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, potentially preventing proper pump programming.
Product
Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1) Administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage
Boston Scientific is recalling 422 units of Malecot Nephrostomy Catheters because they may break at the mid-shaft bond during use.
Product
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting Malecot Catheters are designed for percutaneous drainage within the renal collecting system while maintaining external access. The Stenting Malecot Nephrostomy…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Mid-Shaft Breakage
Boston Scientific is recalling Malecot Nephrostomy Catheter Sets because they are breaking at the mid-shaft bond during use.
Product
Malecot Nephrostomy Catheter Set, Product Number: M0064101010, GTIN: 08714729005278 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V202000·2018-03-28
REV Recalls Motorhomes Due to Potential Satellite Dish Detachment
REV is recalling 2017-2018 motorhomes because satellite dish mounting screws may not be fastened correctly, posing a crash risk if the dish detaches.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, AMERICAN COACH, FLEETWOOD PRODIGY, AMERICAN EAGLE, NAVIGATOR, PULSE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1121-2018·2018-03-28
MedComp Recalls Tesio Catheter Sets Due to Connection Failure Risk
Medical Components, Inc. is recalling 55 Tesio Catheter Sets because potential connection failures could lead to blood loss or air emboli.
Product
12F X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD757, UDI 884908005554 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1136-2018·2018-03-28
Smiths Medical Recalls Medfusion Syringe Pumps Due to Syringe Recognition Issues
Smiths Medical is recalling Medfusion Syringe Pumps because they may fail to recognize or misidentify loaded medication syringes, potentially preventing proper pump programming.
Product
Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps are indicated for the following uses: 1) Administration of fluids requiring precisely controlled infusion rates including blood or blood products, lipids, drugs, antibiotics, enteral solutions and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1126-2018·2018-03-28
MedComp Catheter Repair Kit Recalled for Potential Connection Failures
Medical Components, Inc. is recalling 315 Catheter Repair Kits due to potential connection failures that could cause blood loss or air emboli.
Product
CATHETER REPAIR KIT, REF RMS52001, UDI 884908039658 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0979-2018·2018-03-28
Trader Joe's Peanut Butter Cookies Recalled Due to Mislabeling
Food and Beverage Inc. is recalling Trader Joe's Peanut Butter Sutter's Formula Cookies because they were packed in Chocolate Chip Cookie bags, posing a peanut allergy risk.
Product
Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Weight: 12 oz. (340g) Number of units per package: 16 cookies Package type: Kraft paper bag
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-1120-2018·2018-03-28
MedComp Recalls Tesio Catheter Sets Due to Connection Failure Risk
Medical Components, Inc. is recalling 712 Tesio catheter sets because connection failures could cause blood loss or air emboli.
Product
12F X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR, REF CMD755, UDI 884908005530 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1102-2018·2018-03-28
Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage
Boston Scientific is recalling Re-Entry Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.
Product
Re-Entry" Malecot Nephrostomy Catheter Set, Product Number: M0064101040, GTIN: 08714729008446 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2018·2018-03-28
Beckman Coulter AutoMate 2500 Chemistry Analyzer Recall for Sensor Defect
Beckman Coulter is recalling AutoMate 2550 and 1250 chemistry analyzers because a misaligned sensor may fail to detect missing pipette tips, posing a remote risk of cross-contamination.
Product
AutoMate 2550 "High Speed" Catalog Number ODL25255; AutoMate 1250 "Standard" Catalog Number ODL25125. Chemistry analyzer sample processing and sorting system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1146-2018·2018-03-28
Vascular Insights Recalls ClariVein IC Infusion Catheters Due to Manufacturing Defect
Vascular Insights is recalling 928 ClariVein IC infusion catheters because a manufacturing defect may cause the catheter shaft to delaminate.
Product
ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated for infusion of physician-specified agents into the peripheral vasculature.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0932-2018·2018-03-28
IKEA Recalls Marshmallow Candy Due to Possible Pest Contamination
IKEA is recalling Godis Paskkyckling Marshmallow Candy due to possible pest contamination at the production facility.
Product
Pink flexible, plastic package: Godis Paskkyckling Marshmallow Candy; IKEA; Net Wt. 3.5 oz.; date codes: 10/23/2018 - 01/26/2019; Produced in Sweden for: by IKEA Food Services AB, Almhultsgatan 2, SE-125 86 Malmo, Sweden. Best Before: 10/23/2018 thru 01/26/2019.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1166-2018·2018-03-28
Arrow International Recalls Central Venous Catheter Kits Missing Safety Checklists
Arrow International is recalling 18,124 central venous catheter kits because they lack required safety checklists and procedure notes.
Product
ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venous access to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1161-2018·2018-03-28
Arrow Central Venous Catheter Kits Recalled for Missing Clinical Guides
Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required clinical procedure notes and checklists.
Product
Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions. Permits venous access to central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1164-2018·2018-03-28
Arrow Central Venous Catheter Kits Recalled for Missing Clinical Documentation
Arrow International is recalling 18,124 central venous catheter kits because they lack required clinical guidance documents. The recall is nationwide.
Product
Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1165-2018·2018-03-28
Arrow International Recalls Central Venous Catheter Kits Missing Safety Checklists
Arrow International is recalling 18,124 Pressure Injectable Multi-Lumen CVC Kits because they lack required clinical safety checklists.
Product
Pressure Injectable Multi- Lumen CVC Kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1158-2018·2018-03-28
Arrow International Recalls Percutaneous Sheath Introducer Kits Missing Safety Checklists
Arrow International is recalling 18,124 percutaneous sheath introducer kits because they lack required central line insertion checklists and procedure notes.
Product
Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1159-2018·2018-03-28
Arrow Central Venous Catheter Kits Recalled for Missing Clinical Guidance Documents
Arrow International is recalling 18,124 central venous catheterization kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.
Product
Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access and catheter introduction to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1163-2018·2018-03-28
Arrow Central Venous Catheter Kits Recalled for Missing Safety Checklists
Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required procedural notes and insertion checklists.
Product
Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access to central circulation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1147-2018·2018-03-28
Ethicon Recalls DERMABOND PRINEO Skin Closure System Lots
Ethicon is recalling specific lots of the DERMABOND PRINEO Skin Closure System because the adhesive may not dry within the specified time and may fall off.
Product
DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO System is intended for topical application only to hold closed easily approximated skin edges of wounds from surgical incisions, including punctures from minimally invasive surgery, and simple…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1131-2018·2018-03-28
CooperSurgical 2 MHz Waterproof OB Probe Recalled for Mislabeling
CooperSurgical is recalling 13 units of 2 MHz Waterproof OB probes because they were incorrectly labeled as 3 MHz probes.
Product
Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical 2 MHz Waterproof OB probe is for obstetrical use in the labor and department for late term obstetrical examination associated with larger women. The product detects fetal heart beats as an aid for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1160-2018·2018-03-28
Arrow International Recalls Percutaneous Sheath Introducer Kits Missing Safety Checklists
Arrow International is recalling 18,124 percutaneous sheath introducer kits because they are missing the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.
Product
Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1162-2018·2018-03-28
Arrow Central Venous Catheter Kits Recalled for Missing Safety Checklists
Arrow International is recalling 18,124 central venous catheter kits nationwide because they lack required clinical safety checklists.
Product
Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.
Category
Medical Device
Distribution
Distributed nationwide