State

Rhode Island product recalls

72,940 recalls have nationwide distribution and so reach Rhode Island. 3,043 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,043
Critical: 221
Severe: 570
Most recent: 2026-09-09

Of the 3,043 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 570 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,043 recalls whose distribution notice names Rhode Island specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3401–3425 of 75983

CriticalFDA (Food)·H-0434-2026·2026-02-04
Super greens powder recalled over possible Salmonella Typhimurium contamination
Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.
Product
a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 86001319
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0433-2026·2026-02-04
Super greens powder tubs recalled over possible Salmonella Typhimurium contamination
Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.
Product
Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Gr
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1114-2026·2026-02-04
Pediatric emergency tapes recalled over potentially harmful drug dosing errors
SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1117-2026·2026-02-04
Filled Broselow organizers recalled over potentially harmful dosing errors
SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Comp
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V066000·2026-02-04
Freightliner M2 steering gearboxes may have been assembled with insufficient oil
Fontaine Modification is recalling certain 2024-2025 Freightliner Business Class M2 vehicles because the steering gearbox assembly may have been assembled with insufficient oil.
Product
FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1170-2026·2026-02-04
Lemon ginger hibiscus beer recalled over possibly unpasteurized ginger juice
Weaver's Brew is recalling 1,014 cases of Goldenroot Lemon Ginger Hibiscus Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Product
Genesis Knotless Anchor
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1184-2026·2026-02-04
Pregnancy tests recalled over rodent activity in a distribution center
Gold Star Distribution is recalling pregnancy tests over potential exposure of rodents and rodent activity in its distribution center.
Product
PREGNANCY TEST 24CT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0299-2026·2026-02-04
Methylprednisolone dose packs recalled over misoriented blister foil dosing information
Greenstone is recalling 3,456 cartons of methylprednisolone tablets Dosepak, 4 mg, because the blister foil was applied in the wrong orientation, giving incorrect dosing information.
Product
METHYLPREDNISOLONE — METHYLPREDNISOLONE (METHYLPREDNISOLONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1206-2026·2026-02-04
Ingenia 1.5T systems recalled over elastography stiffness value errors
Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1185-2026·2026-02-04
Conductivity standard solutions recalled over incorrect dialysate conductivity values
NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.
Product
Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity Standard Solutions are a secondary standard solution used for the calibration of conductivity cells together with conductivity meters
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1219-2026·2026-02-04
Central line dressing kits recalled over open swabstick applicator seals
LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.
Product
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1188-2026·2026-02-04
Bandages and first aid kits recalled over rodent activity in storage
Gold Star Distribution is recalling first aid kits and bandages over potential exposure of rodents and rodent activity in its distribution center.
Product
Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L; 3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B; 4) PACEMAKER SET UP, Kit SKU DYNJ63377D; 5) PACK PACEMAKER CUSTOM,9909178, Ki
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1213-2026·2026-02-04
Hybrid suture anchors recalled after reports of breakage and pull out
Aju Pharm is recalling 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Product
MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1179-2026·2026-02-04
Q.namix R fluoroscopy systems recalled over unflipped and mismatched images
Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Product
Alphenix INFX-8000V, interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2026·2026-02-04
Ingenia 3.0T CX systems recalled over elastography stiffness value errors
Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1181-2026·2026-02-04
Condoms recalled over rodent activity in a distribution center
Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.
Product
Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1211-2026·2026-02-04
Ingenia Elition S systems recalled over elastography stiffness value errors
Philips North America is recalling 5 units of the Ingenia Elition S because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1116-2026·2026-02-04
MR 7700 systems recalled over elastography stiffness value errors
Philips North America is recalling 9 units of the MR 7700 MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1216-2026·2026-02-04
SmartPath dStream upgrades recalled over elastography stiffness value errors
Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Product
SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1215-2026·2026-02-04
SmartPath dStream 3.0T upgrades recalled over elastography stiffness errors
Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Product
SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1210-2026·2026-02-04
Ingenia Ambition X systems recalled over elastography stiffness value errors
Philips North America is recalling 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1204-2026·2026-02-04
Evolution Upgrade 1.5T systems recalled over elastography stiffness value errors
Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Product
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1167-2026·2026-02-04
Biocomposite suture anchors recalled after reports of breakage and bending
Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Product
Fixone Biocomposite Anchor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1183-2026·2026-02-04
Toothbrushes recalled over rodent activity in a distribution center
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
Product
Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1175-2026·2026-02-04
Q.namix T fluoroscopy systems recalled over unflipped and mismatched images
Siemens is recalling 7 units of the LUMINOS Q.namix T fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Product
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Version VB10D-SP02
Category
Medical Device
Distribution
Distributed nationwide