State

Rhode Island product recalls

73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,053
Critical: 221
Severe: 707
Most recent: 2026-10-28

Of the 3,053 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 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39201–39225 of 76794

SevereFDA (Drugs)·D-0965-2018·2018-07-25
Avella Recalls Phenylephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 40 bags of Phenylephrine 10 mg due to potential leakage that compromises sterility. The product was distributed nationwide.
Product
PHENYLephrine 10 mg (PHENYLephrine HCL (USP) 10mg, 0.9% Sodium Chloride (USP) 250 mL. Volume: 251 mL Single dose bag. For: Redlands Community Hospital Pharmacy. BY: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 NDC 15082-856-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2514-2018·2018-07-25
Medtronic Recalls Tri-Staple 2.0 Curved Tip Intelligent Reloads
Medtronic is recalling specific Tri-Staple 2.0 Curved Tip Intelligent Reloads because a missing sled component may prevent staple formation, potentially leading to bleeding or leakage.
Product
Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system 30 mm Vascular/Medium, Item Code SIG30ACTAVM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2509-2018·2018-07-25
Medtronic Endo GIA Vascular Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 45mm Vascular Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA 45mm Gray Articulating Vascular Reload with Tri-Staple Technology, Item Code EGIA45AV
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2506-2018·2018-07-25
Endo GIA 60 mm Articulating Vascular/Medium Loading Unit Recalled for Missing Sled
COVIDIEN MEDTRONIC is recalling Endo GIA 60 mm Articulating Vascular/Medium Loading Units because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple Technology, Item Code EGIA60AVM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0959-2018·2018-07-25
Avella Recalls Norepinephrine Syringes Due to Potential Sterility Compromise
Avella of Deer Valley, Inc. is recalling 850 single-dose norepinephrine syringes nationwide due to potential bag leakage that may compromise sterility.
Product
NORepiNEPHrine Bitartrate, USP 160 mcg in 5% Dextrose, USP QS 10mL. Volume 10mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-807-61
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2511-2018·2018-07-25
Medtronic Endo GIA Stapler Recall Due to Missing Sled Component
Medtronic is recalling Endo GIA staplers that may be missing a sled component, which could cause staple line failure, bleeding, or leakage during surgery.
Product
Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple Technology, Item Code EGIA454AVM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0961-2018·2018-07-25
Avella Recalls Norepinephrine Bags Due to Potential Leakage
Avella of Deer Valley is recalling 1,290 bags of Norepinephrine Bitartrate 4 mg due to potential leakage and lack of sterility assurance.
Product
NORepiNEPHrine4mg (Norepinephrine Bitartrate (USP) 4 mg added to 0.9% Sodium Chloride (USP) 250 mL Volume: 254 mL Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-860-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0947-2018·2018-07-25
Avella Recalls Heparin Bags Due to Potential Sterility Issues
Avella of Deer Valley is recalling 900 bags of Heparin 12,500 Units in 5% Dextrose due to potential bag leakage and lack of sterility assurance.
Product
HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume: 252.5 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue Phoenix, AZ 85085. NDC 42852-745-25
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V481000·2018-07-25
Forest River Recalls 2017-2018 Glaval Transit Buses for Seat Belt Defect
Forest River is recalling 2017-2018 Glaval transit buses because a washer in the seat belt assembly may break, allowing the belt to separate from the vehicle.
Product
GLAVAL BUS — GLAVAL BUS LEGACY, CONCORDE II, COMMUTE, APOLLO
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0952-2018·2018-07-25
Avella Recalls Magnesium Sulfate Bags Due to Sterility Concerns
Avella of Deer Valley is recalling 175 bags of Magnesium Sulfate in Sodium Chloride due to potential bag leakage and lack of sterility assurance.
Product
MAGnesium 2gm in NS 100 mL (MAGnesium SULfate (USP) 2 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 104 mL. Single dose bag. For: Desert Regional Med Ctr By: Avella of Houston, 9256 Kirby Dr., Houston, TX 77054. NDC: 42852-907-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2502-2018·2018-07-25
Maquet VOLISTA StandOP Surgical Light Recall for Detachment Risk
Maquet is recalling 151 VOLISTA StandOP surgical lights due to a potential light head detachment issue that could cause serious injury.
Product
VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF AIM STP; ARD568821911 VLT600SF AIM STP QL; ARD568821910 VLT600SF STP QL; ARD568811901 VLT600SF AIM STP Product Usage: The Maquet VOLISTA…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0939-2018·2018-07-25
Avella Recalls Norepinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 4,280 bags of Norepinephrine 8 mg due to potential bag leakage and lack of assurance of sterility.
Product
NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to 5% Dextrose Inj. (USP) 250 mL. (Concentration 32 mcg/mL) Volume: 258 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-815-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0964-2018·2018-07-25
Avella Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 225 syringes of ePHEDrine Sulfate due to potential bag leakage and lack of sterility assurance.
Product
ePHEDrine Sulfate, USP 50 mg in 0.9% Sodium Chloride, USP QS 10mL. 50 mg/10 mL (5 mg per mL). Volume 10 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-895-61
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2512-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 45mm reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple Technology, Item Code EGIA45CTAVM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0940-2018·2018-07-25
Avella Recalls Phenylephrine Bags Due to Potential Leakage
Avella of Deer Valley is recalling 200 bags of Phenylephrine 40 mg due to potential leakage that compromises sterility.
Product
PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj., USP 250 mL) Volume: 254 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-893-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0936-2018·2018-07-25
Avella Recalls Magnesium Sulfate Bags Due to Sterility Concerns
Avella of Deer Valley is recalling 100 bags of Magnesium Sulfate in Sodium Chloride due to potential bag leakage and lack of sterility assurance.
Product
MAGnesium 4gm in NS 100 mL (MAGnesium SULfate (USP) 4 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 108 mL. Single dose bag. For: Gaston Memorial Hospital By: Avella of Houston, 9256 Kirby Dr., Houston, TX 77054. NDC: 42852-905-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0960-2018·2018-07-25
Avella Recalls Norepinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 2,280 bags of Norepinephrine Bitartrate in 5% Dextrose due to potential bag leakage and lack of sterility assurance.
Product
NORepiNEPHrine4mg (Norepinephrine Bitartrate (USP) 4 mg added to 5% Dextrose Inj. (USP) 250 mL (Concentration 16 mcg/mL) Volume: 254 mL Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-807-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0938-2018·2018-07-25
Avella Recalls Morphine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 1,500 bags of Morphine 1 mg/mL due to potential bag leakage and lack of assurance of sterility.
Product
MORphine 1 mg/mL (Morphine Sulfate, USP 100mg, 0.9% Sodium Chloride, USP QS 100 mL). Volume 100 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-241-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0929-2018·2018-07-25
Avella Recalls CeFAZolin Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 2,500 bags of ceFAZolin 2 gm in NS 100mL due to potential bag leakage that compromises sterility.
Product
ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm, 0.9% Sodium Chloride (USP) 100mL. Volume 110 mL. Single dose bag. Avella of Houston 9265 Kirby Dr., Houston, TX 77054 NDC: 42852-604-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2516-2018·2018-07-25
Medtronic Tri-Staple 2.0 Curved Tip Reloads Recalled for Missing Sled Component
Medtronic is recalling Tri-Staple 2.0 Curved Tip Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system , Item Code EGIA30CTAV
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0937-2018·2018-07-25
Avella Recalls Midazolam Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 1,860 bags of Midazolam 1 mg/mL due to potential bag leakage and lack of assurance of sterility.
Product
Midazolam 1 mg/mL (Midazolam HCL (USP) 100 mg, Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston TX 77054. NDC 4252-401-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2503-2018·2018-07-25
Endo GIA 45 mm Articulating Medium/Thick Reload Recalled for Missing Sled Component
COVIDIEN MEDTRONIC is recalling Endo GIA 45 mm Articulating Medium/Thick Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology, Item Code EGIA45AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2510-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 45 mm Extra Thick Black Articulating Reloads because a missing sled component may prevent staple formation, potentially leading to bleeding or leakage.
Product
Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple Technology, Item Code EGIA45AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0957-2018·2018-07-25
Avella Recalls Midazolam Syringes Due to Sterility Assurance Concerns
Avella of Deer Valley, Inc. is recalling 110 syringes of Midazolam 1 mg/mL due to a lack of assurance of sterility and potential bag leakage.
Product
Midazolam 1 mg/mL (Midazolam HCL (USP) 55 mg, 0.9% Sodium Chloride, (USP) QS 55 mL) Volume: 55mL. Single dose syringe. Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-401-76
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0958-2018·2018-07-25
Avella Recalls NORepiNEPHrine 16 Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 520 bags of NORepiNEPHrine 16 injection due to potential bag leakage and lack of assurance of sterility.
Product
NORepiNEPHrine 16 (NORepiNEPHrine Bitartrate (USP) 16 mg, 5% Dextrose Inj. (USP) 250 mL. Volume: 266 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-834-25
Category
Drug
Distribution
Distributed nationwide