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.

46976–47000 of 76871

HighFDA (Devices)·Z-0776-2017·2016-12-28
AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk
AngioDynamics is recalling 145 boxes of Stiffened Micro-Introducer Kits because the sheath/dilator components may have a rotating luer that detaches during use.
Product
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T NON-ECHO S PG, Item Number H787065970655, Catalog No.REF 06597065, 2) 4 F Stiffened Micro-Introducer Kit, STF 4F M.I. KIT 45CM NT/T NON-ECHO S PG, Item Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0898-2017·2016-12-28
Teleflex Recalls Mucosal Atomization Devices Due to Incomplete Atomization
Teleflex Medical is recalling Mucosal Atomization Devices because they may produce a straight stream instead of a fully atomized plume of medication.
Product
Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code MAD100, MAD100OS MAD110, MAD110OS, MAD130, MAD130OS, MAD140, MAD140OS, MAD300, MAD300B. Manufactured By: Wolfe-Tory Medical, Inc., Teleflex Medical. For…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V954000·2016-12-28
Keystone Recalls 2016-2017 Alpine and Avalanche Fifth-Wheel Trailers for Label Error
Keystone is recalling 2016-2017 Alpine and Avalanche fifth-wheel trailers because the Federal Placard may list incorrect spare tire load range information, potentially leading to overinflation.
Product
KEYSTONE — KEYSTONE AVALANCHE, ALPINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V938000·2016-12-28
Navistar Recalls 2017 International Trucks Due to Battery Latch Fire Risk
Navistar is recalling 2017 International ProStar, LoneStar, 9900i, and TranStar trucks because a battery latch may cause an electrical short and fire.
Product
INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, 9900I, TRANSTAR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0784-2017·2016-12-28
Ultroid Procedure Pack Recalled for Quality System Non-Compliance
Ultroid Technologies is recalling 52,084 procedure packs because they were not manufactured under required quality system controls.
Product
Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes.
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-0877-2017·2016-12-28
BD SurePath Collection Vials Recalled Due to Cracked Caps
Becton Dickinson is recalling SurePath collection vials because cracked caps may allow preservative fluid to leak.
Product
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed for use with the PrepStain¿ System. SurePath¿ Preservative Fluid is an alcohol-based, preservation solution that serves as a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0774-2017·2016-12-28
AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk
AngioDynamics is recalling 751 Stiffened Micro-Introducer Kits because a component may detach during use.
Product
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970505, Catalog No.REF 06597050, 2) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970525, Catalog…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0870-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8470-009-030 3.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0812-2017·2016-12-28
Brownwood Farms Recalls BBQ Mustard Glaze for Undeclared Soy
Brownwood Farms is recalling BBQ Mustard Glaze because it contains soy ingredients not declared on the label.
Product
Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Barbeque Mustard 11oz)
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2017·2016-12-28
Nuvectra Recalls Algovita Spinal Cord Stimulation Leads Due to Stylet Protrusion
Nuvectra is recalling Algovita Spinal Cord Stimulation System percutaneous leads because the stylet may protrude beyond the distal lead tip.
Product
Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Leads, 12-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Trial Leads, 8-electrode…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0886-2017·2016-12-28
Amendia Recalls Black Widow Spinal Plates Due to Mating Feature Defect
Amendia, Inc. is recalling 48 units of Black Widow Buttress Plates due to a design defect in the mating feature between the plate and screw.
Product
Black Widow Plate 19mm Plate, Part Number TBP119; Black Widow Plate 23mm Plate, Part Number TBP123 The Black Widow Buttress Plates and Screws are designed for preventing migration or expulsion of allograft or autograft in the thoracolumbar to S1 Spinal region
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0230-2017·2016-12-28
Sage Products Recalls Comfort Shield Barrier Cream Cloths Due to CGMP Deviations
Sage Products LLC is recalling Comfort Shield Barrier Cream Cloths due to CGMP deviations and potential contamination on shared equipment.
Product
COMFORT SHIELD BARRIER — COMFORT SHIELD BARRIER (DIMETHICONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0869-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8450-107-525 2.5MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0871-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8470-009-040 4.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0785-2017·2016-12-28
Ultroid Sterile Disposable Probes Recalled for Quality System Non-Compliance
Ultroid Technologies is recalling 7,784 sterile disposable probes because they were not manufactured under required quality system controls.
Product
Ultroid Sterile Disposable Probes sold individually
Category
Medical Device
Distribution
34 states
ModerateFDA (Food)·F-0816-2017·2016-12-28
Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Yellow #5
Brownwood Farms is recalling Jalapeno Cherry Butter because it contains Yellow #5, an ingredient not declared on the label.
Product
Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0813-2017·2016-12-28
Brownwood Farms Apple Riesling Salsa Recalled for Undeclared Yellow 5
Brownwood Farms is recalling Apple Riesling Salsa because it contains Yellow 5, an ingredient not declared on the label.
Product
Brownwood Farms Apple Riesling Salsa. 21oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Apple Riesling Salsa 21oz). Kimmel Orchard & Vineyard (Apple Riesling Salsa 21oz). St. Julian Winery (Apple Riesling Salsa 19oz).
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0873-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8450-009-030 3.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0814-2017·2016-12-28
Brownwood Farms Peach Salsa Recalled for Undeclared Yellow 5 Ingredient
Brownwood Farms is recalling Peach Salsa because it contains Yellow 5, a color additive not declared on the label.
Product
Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers Harbor Vineyard (Peach Salsa 12oz). Crossroads.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0824-2017·2016-12-28
Stanmore Implants Recalls DF Coated Integral Shaft and Stem Components
Stanmore Implants Worldwide Ltd. is recalling 15 units of DF Coated Integral Shaft & Stem components due to packaging punctures reported by customers.
Product
DF Coated Integral Shaft & Stem 15x30x38; DF Coated Integral Shaft & Stem 15x36x44; DF Coated Integral Shaft & Stem 30x30x38; DF Coated Integral Shaft & Stem 30x36x44 The product is a component is a systems that is intended for the replacement if diseased or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0771-2017·2016-12-28
Teleflex Recalls RUSCH Pocket PAC Intermittent Catheter Kits Due to Labeling Error
Teleflex Medical is recalling RUSCH Pocket PAC Intermittent Catheter Kits because they are labeled with expiration dates that exceed the validated shelf life.
Product
RUSCH, Pocket PAC IC Intermittent Cath Kit, 8 FR, 12 FR, 14 FR, 10 FR and 16 FR, Rx Only, Sterile, Intermittent self-catheterization
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0772-2017·2016-12-28
AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk
AngioDynamics is recalling 162 boxes of Stiffened Micro-Introducer Kits because the rotating luer may detach from the dilator hub during use.
Product
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS ECHO B PG, Item Number H787065970395, Catalog No.REF 06597039, 2) 5 F Stiffened Micro-Introducer Kit, STF 5F M.I. KIT 45CM SS/SS ECHO S PG, Item Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0820-2017·2016-12-28
Stanmore Tibial Component Fixed Hinge Recall Due to Pouch Puncture
Stanmore Implants Worldwide Ltd. is recalling 13 units of Tibial Component Fixed Hinge Small Long and Short due to punctured packaging.
Product
Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0231-2017·2016-12-28
Sage Products Recalls Chlorhexidine Gluconate Cloth Due to CGMP Deviations
Sage Products LLC is recalling 2% Chlorhexidine Gluconate Cloth due to CGMP deviations and potential contamination. The product was distributed nationwide and internationally.
Product
CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0384-2017·2016-12-28
Teleflex Medical Recalls LMA MADgic Atomization Devices for Spray Defect
Teleflex Medical is recalling LMA MADgic atomization devices because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
LMA MADgic, Atomization Device with 3mL Syringe, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce…
Category
Medical Device
Distribution
Distributed nationwide