State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46151–46175 of 76871

SevereFDA (Drugs)·D-0499-2017·2017-03-08
United Exchange Recalls Eye Wash Bottles Due to Sterility Concerns
United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.
Product
EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0788-2017·2017-03-08
Medtronic SynchroMed II Software Card Recall for Priming Bolus Function
Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.
Product
Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0497-2017·2017-03-08
United Exchange Recalls Eye Irrigating Solution Due to Sterility Concerns
United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.
Product
Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0498-2017·2017-03-08
United Exchange Eye Wash Recalled Due to Lack of Sterility Assurance
United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.
Product
Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V151000·2017-03-08
Volkswagen Recalls 2007-2010 Touareg for Fuel Filter Flange Crack Risk
Volkswagen is recalling 2007-2010 Touareg vehicles because a fuel filter flange may crack and leak fuel, increasing the risk of fire.
Product
VOLKSWAGEN — VOLKSWAGEN TOUAREG
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0491-2017·2017-03-08
Mylan Recalls Glipizide Extended-Release Tablets Due to Foreign Tablet Presence
Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.
Product
glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1252-2017·2017-03-08
Olympus Uretero-reno Videoscope Recall Due to Insertion Tube Breakage
Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.
Product
Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1384-2017·2017-03-08
Beckman Coulter iChemVELOCITY Urine Chemistry System Recalled for Probe Misalignment
Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.
Product
iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1388-2017·2017-03-08
Cook Inc. Recalls Check-Flo Performer Introducer Sets Due to Blood Loss Risk
Cook Inc. is recalling 854 Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.
Product
Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1255-2017·2017-03-08
Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias
Siemens is recalling specific Calibrator A Kits due to a negative bias in FT4 assays and potential calibration failures on certain systems.
Product
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1392-2017·2017-03-08
Cook Inc. Recalls Check-Flo Introducer Devices Due to Blood Loss Reports
Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.
Product
Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1389-2017·2017-03-08
Cook Inc. Recalls Check-Flo Hemostasis Assemblies Due to Blood Loss Reports
Cook Inc. is recalling 1,589 Check-Flo Hemostasis Assemblies because reports indicate increased blood loss associated with the device's valve design.
Product
Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1387-2017·2017-03-08
Cook Inc. Recalls Check-Flo Performer Introducers Due to Blood Loss Reports
Cook Inc. is recalling 884 Check-Flo Performer Introducers because a specific valve design is associated with increased reports of blood loss.
Product
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1393-2017·2017-03-08
Cook Inc. Recalls TriForce Peripheral Crossing Sets Due to Blood Loss Reports
Cook Inc. is recalling 1,875 TriForce Peripheral Crossing Sets because a specific valve design is associated with increased reports of blood loss.
Product
TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood vessels and support a wire guide while performing percutaneous peripheral…
Category
Medical Device
Distribution
46 states
HighNHTSA·17V150000·2017-03-08
Audi Recalls 2017 A5 and S5 Cabriolets for Seat Belt Pretensioner Defect
Volkswagen Group of America is recalling 2017 Audi A5 and S5 Cabriolets because a seat belt pretensioner component may detach during a crash, creating a projectile hazard.
Product
AUDI — AUDI S5 CABRIOLET, A5 CABRIOLET
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1391-2017·2017-03-08
Cook Inc. Recalls Micropuncture Check-Flo Performer Introducer Sets Due to Blood Loss
Cook Inc. is recalling 778 Micropuncture Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.
Product
Micropuncture Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1390-2017·2017-03-08
Cook Inc. Recalls Flexor Radial Access Sets Due to Blood Loss Reports
Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.
Product
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1385-2017·2017-03-08
Merge Healthcare Recalls Unity PACS Software Due to Image Error
Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.
Product
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1386-2017·2017-03-08
Maquet CARDIOSAVE IABP Li-Ion Battery Recall Due to Venting Risk
Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.
Product
CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0508-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) 30 mg capsules because they failed to meet dissolution specifications.
Product
Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0502-2017·2017-03-08
Sun Pharmaceutical Recalls Alfuzosin Hydrochloride Tablets Due to Foreign Matter
Sun Pharmaceutical Industries is recalling specific lots of Alfuzosin Hydrochloride Extended-release Tablets because a consumer complaint identified a broken piece of wire rope embedded in a tablet.
Product
ALFUZOSIN HYDROCHLORIDE — ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2017·2017-03-08
Cyclosporine Capsules Recalled for Impurity Specification Failures
Amerisource Health Services is recalling 454 cartons of Cyclosporine Capsules, 100 mg, due to failed impurity specifications.
Product
CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0506-2017·2017-03-08
Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The affected lot is distributed nationwide.
Product
ZENATANE — ZENATANE (ISOTRETINOIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1395-2017·2017-03-08
MED-EL SONNET Mini Battery Pack Cable Recall for Welding Defect
MED-EL is recalling 538 SONNET Mini Battery Pack Cables because the compartment lock was not firmly welded to the housing.
Product
SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external battery pack used to power one MED-EL SONNET control unit. It can be worn on the upper body or the hip using different SONNET Mini…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1256-2017·2017-03-08
Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias
Siemens is recalling specific Calibrator A kits due to confirmed negative bias and potential calibration failures for the FT4 assay on certain ADVIA Centaur systems.
Product
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
Category
Medical Device
Distribution
Distributed nationwide