State

Rhode Island product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1401–1425 of 75950

SevereFDA (Devices)·Z-2276-2026·2026-06-10
B. Braun spinal needle kits recalled over Huons bupivacaine quality issues
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Product
Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2252-2026·2026-06-10
BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1015-2026·2026-06-10
Imitation Cajun crab seafood salad does not declare crab and pollock
Albertsons store-made Seafood Salad Imitation Cajun Crab is being recalled because the contains statement does not declare crab and pollock. 53 units are affected.
Product
UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2026·2026-06-10
Phothera 200 phototherapy calibration certificates had outputs reversed
Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.
Product
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0579-2026·2026-06-10
TopCare ultra strength antacid tablets contain small metallic particles
TopCare Health Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT — TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2026·2026-06-10
Philips Azurion 7B12 Roadmap Pro may produce unusable dark images
Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2026·2026-06-10
Stapes prosthesis pistons carry an incorrect functional length on labeling
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Product
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0562-2026·2026-06-10
Casey's extra strength antacid tablets contain small metallic particles
Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.
Product
Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2284-2026·2026-06-10
Philips Azurion 3M12 Roadmap Pro may produce unusable dark images
Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2282-2026·2026-06-10
Neptune docking station shipped without verified electrical safety testing
A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.
Product
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0955-2026·2026-06-10
Albertsons cravin carrot cake does not declare pecan allergen
Albertsons store-made Cake Cravin Carrot 8-inch 1-layer is being recalled because the contains statement does not declare pecan. 138 units are affected.
Product
UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's store-made item and is sold by each unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0978-2026·2026-06-10
Albertsons sub sandwich tray does not declare pistachio allergen
Albertsons store-made Kitchen Tray Sub Sandwich is being recalled because the contains statement does not declare pistachio. 13 units are affected.
Product
UPC 29259700000 KITCHEN TRAY SUB SANDWICH SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1017-2026·2026-06-10
Albertsons apple waldorf salad does not declare walnut allergen
Albertsons store-made Apple Waldorf Salad is being recalled because the contains statement does not declare walnut. 33 units are affected.
Product
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000 Kitchen SALAD APPLE WALDORF LRG UPC 27170300000 Kitchen SALAD APPLE WALDORF MED UPC 27169300000 Kitchen SALAD APPLE W
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2026·2026-06-10
Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Product
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1025-2026·2026-06-10
Pad Thai chicken with pot stickers does not declare anchovy
Albertsons store-made Ready Meals Wok Pad Thai Chicken with Pot Stickers is being recalled because the contains statement does not declare anchovy. 39 units are affected.
Product
UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2302-2026·2026-06-10
BD Pyxis MedStation fingerprint scanners may overheat and cause burns
BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2026·2026-06-10
Philips Azurion 5M20 Roadmap Pro may produce unusable dark images
Philips Azurion 5M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0569-2026·2026-06-10
Family Wellness ultra strength antacid tablets contain metallic particles
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
Product
FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0574-2026·2026-06-10
GoodSense antacid chewable tablets contain small metallic particles
GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.
Product
GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1022-2026·2026-06-10
Albertsons fresh berry and chicken salad does not declare walnut
Albertsons store-made Ready Meals Salad Fresh Berry & Chicken is being recalled because the contains statement does not declare walnut. 228 units are affected.
Product
UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0988-2026·2026-06-10
Albertsons 16-inch carving tray does not declare walnut
An Albertsons store-made 16-inch carving tray is being recalled because the contains statement does not declare walnut. 12 units are affected.
Product
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0554-2026·2026-06-10
Spectra lidocaine ampules recalled over lack of sterility assurance
Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0576-2026·2026-06-10
Equaline extra strength antacid tablets contain small metallic particles
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID — EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0571-2026·2026-06-10
Hy-Vee extra strength antacid tablets contain small metallic particles
Hy-Vee Extra Strength Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0982-2026·2026-06-10
Pavilions single serve banana nut muffins do not declare walnut
Pavilions Banana Nut Muffins single serve, an Albertsons store-made item, are being recalled because the contains statement does not declare walnut. 55 units are affected.
Product
UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide