State

Rhode Island product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44676–44700 of 76863

SevereFDA (Devices)·Z-2275-2017·2017-06-14
Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk
Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions requiring central venous…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2278-2017·2017-06-14
Arrow International Recalls Multi-Lumen CVC Kits Due to Needlestick Risk
Arrow International is recalling specific multi-lumen central venous catheter kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Product
AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2287-2017·2017-06-14
Arrow International Recalls Access Kits Due to Needlestick Injury Risk
Arrow International is recalling Access Kits with Maximal Barrier Precautions because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Product
Arrow¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2272-2017·2017-06-14
Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk
Arrow International is recalling certain central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2289-2017·2017-06-14
Arrow Access Kit Recalled Due to Needlestick Injury Risk
Arrow International is recalling specific Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Product
Arrow¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2286-2017·2017-06-14
Arrow PICC Recall Due to Safety Cover Disengagement and Needlestick Risk
Arrow International is recalling Arrow PICC devices with Chlorag+ard Technology because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Arrow PICC with Chlorag+ard Technology The ArrowEVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for intravenous therapy, blood sampling…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2261-2017·2017-06-14
Arrow Percutaneous Sheath Introducer Kit Recalled for Needlestick Injury Risk
Arrow International is recalling Percutaneous Sheath Introducer Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5-8 Fr. Catheters. The Arrow Percutaneous Sheath Introducer permits venous access and catheter…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2331-2017·2017-06-14
Krisppee Clam Fry Mix Recalled for Undeclared Milk Allergen
Krisppee Products Co. is recalling Clam Fry Mix in 5, 25, and 50 lb sizes because the product contains undeclared milk.
Product
KRISPPE CLAM-FRY-MIX NET WEIGHT 5 lbs., 25 lbs., 50 lbs.
Category
Food
Distribution
2 states
SevereNHTSA·17V380000·2017-06-14
Piaggio Recalls 2016-2017 Moto Guzzi Motorcycles for Brake Hose Defect
Piaggio is recalling 2016-2017 Moto Guzzi motorcycles because the front ABS brake hose may rub against the engine, causing a fluid leak that increases crash risk.
Product
PIAGGIO — PIAGGIO, MOTO GUZZI V7 III SPECIAL 750, MOTO GUZZI V7 III RACER 7, V9 BOBBER, V7 III STONE 750
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2333-2017·2017-06-14
Krisppee Batter Mix Recalled for Undeclared Milk Allergen
Krisppee Products Co. is recalling Krisppee Batter Mix for Fish & Chips due to undeclared milk. The product was distributed in Rhode Island and Massachusetts.
Product
KRISPPE BATTER MIX For FISH & CHIPS Net WEIGHT 5 lbs., 25 lbs., 50 lbs.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2285-2017·2017-06-14
Arrow PICC Kit Recalled Due to BD Eclipse Needle Safety Cover Issues
Arrow International is recalling certain PICC kits because the packaged BD Eclipse Needle has a safety cover that may disengage, posing a needlestick injury risk.
Product
Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure Injectable P1CC with Chlorag+ard Antimicrobial and Antithrombogenic Technology is indicated for short-term or long-term peripheral access to the central venous system for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2273-2017·2017-06-14
Arrow International Recalls Central Venous Catheter Kits Due to Needlestick Risk
Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2300-2017·2017-06-14
Arrow Arterial Catheterization Kit Recalled for Needlestick Injury Risk
Arrow International is recalling Arterial Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2295-2017·2017-06-14
Arrow International Recalls Femoral Arterial Line Catheterization Kits
Arrow International is recalling specific femoral arterial line catheterization kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2267-2017·2017-06-14
Arrow International Recalls Central Catheters Due to Needlestick Injury Risk
Arrow International is recalling 43,394 units of central catheters because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Pressure injectable Jugular Axillo-Subclavian Central CThe CG+Arrow JACC powered by Arrow VPS Stylet permits venous access to the central circulation through a central veinatheter (JACC) Product
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2266-2017·2017-06-14
Arrow PICC Recall Initiated Due to Needlestick Injury Risk
Arrow International is recalling 43,394 units of Arrow PICC with Chlorag+ard Technology due to safety cover disengagement and needlestick injury risks associated with packaged BD Eclipse Needles.
Product
Arrow PICC with Chlorag+ard Technology A PICC permits venous access to the central circulation through a peripheral vein
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2257-2017·2017-06-14
Arrow VPS Access Kit Recalled for Needlestick Injury Risk
Arrow International is recalling VPS Access Kits due to safety cover disengagement on packaged BD Eclipse Needles, posing a needlestick injury risk.
Product
Arrow VPS Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally inserted Central Venous Catheter The Arrow(r) CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2293-2017·2017-06-14
Arrow Percutaneous Sheath Introducer Kit Recalled for Needlestick Injury Risk
Arrow International is recalling specific Percutaneous Sheath Introducer Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7 - 7.5¿¿Fr. Catheters The Arrow Percutaneous Sheath Introducer permits venous access and catheter introduction to the central ciruclation
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2304-2017·2017-06-14
Arrow Percutaneous Sheath Introducer Kit Recalled for Needlestick Injury Risk
Arrow International is recalling Percutaneous Sheath Introducer Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5-8 Fr. Catheters The Arrow¿ Percutaneous Sheath Introducer permits venous access and catheter…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2292-2017·2017-06-14
Arrow International Recalls Central Catheters Due to Needlestick Injury Risk
Arrow International is recalling specific central catheters because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
"Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC) Product" The CG+ Arrow JACC powered by Arrow VPS Stylet permits venous access to the central circulation through a central vein. The VPS Stylet, used with the VPS Console, quickly and accurately guides the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2291-2017·2017-06-14
Arrow PICC Recall Initiated Due to Safety Cover Disengagement and Needlestick Injury
Arrow International is recalling Arrow PICC products with Chlorag+ard Technology due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Arrow PICC with Chlorag+ard Technology A PICC permits venous access to the central circulation through a peripheral vein. The intended use of the VP'S Stylet and Console (VPS System) is to quickly and accurately guide market available central catheters to the desired location…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2297-2017·2017-06-14
Arrow Radial Artery Catheterization Kit Recalled for Needlestick Injury Risk
Arrow International is recalling Radial Artery Catheterization Kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2264-2017·2017-06-14
Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk
Arrow International is recalling 43,394 central venous access kits because the packaged BD Eclipse Needle has a safety cover that may disengage, posing a needlestick injury risk.
Product
ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit. The MAC Two-Lumen Central Venous Access Device with ARROWg+ard Blue permits venous access and catheter introduction to the central circulation
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2282-2017·2017-06-14
Arrow VPS Access Kit Recalled for Needlestick Injury Risk
Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Product
Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2335-2017·2017-06-14
Still Riding Foods Recalls Gluten-Free Pizza Crust Due to Botulism Risk
Still Riding Foods is recalling gluten-free pizza crust due to a C. botulinum hazard in vacuum-packed products. The recall covers 1,555 cases distributed across 23 states.
Product
STILL RIDING FOODS GLUTEN FREE PIZZA CRUST; Sold in the following package sizes: 36/9" NET WT 15lbs (6.80kg); 12/12" NET WT 10lbs (5.44kg); 24/12" NET WT 27lbs (12.25kg); 18/9" NET WT 7lbs (3.18kg)
Category
Food
Distribution
24 states