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.

1201–1225 of 75950

ModerateFDA (Drugs)·D-0635-2026·2026-06-24
Med Pride bacitracin zinc packets recalled over manufacturing practice deviations
Med Pride Bacitracin Zinc Ointment, 500 units in 0.9 g packets, is being recalled because of CGMP deviations observed during an FDA inspection. 1,087 tubes affected.
Product
Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets Net Wt 130g, 144 count box, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30352 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2436-2026·2026-06-24
Medline ACDF and ACL procedure kits contain recalled Mastisol adhesive
Medline convenience kits for ACD, ACDF, ACL and ALIF procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYN
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0603-2026·2026-06-24
Burkhart benzocaine topical anesthetic gel bottles may have incomplete seals
Burkhart topical anesthetic gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.
Product
BURKHART TOPICAL ANESTHETIC — BURKHART TOPICAL ANESTHETIC (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0591-2026·2026-06-24
Kerr Insta-Char activated charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char activated charcoal in a sorbitol base with cherry flavor is being recalled because the product did not meet the Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2429-2026·2026-06-24
Medline labor and delivery C-section kits contain recalled Mastisol adhesive
The Medline Labor & Delivery C-Section convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2427-2026·2026-06-24
Medline hernia repair totes contain recalled Mastisol liquid adhesive
The Medline Hernia Repair Tote convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2460-2026·2026-06-24
directCHECK whole blood control labeled with incorrect performance range
directCHECK ACT-LR whole blood quality control, level 2, is being recalled because the assayed control carries labeling with an incorrect performance range. 6,060 units affected.
Product
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2447-2026·2026-06-24
Medline hysterectomy packs contain recalled Mastisol liquid adhesive
The Medline Hysterectomy Pack-LF is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0638-2026·2026-06-24
Med Pride clotrimazole antifungal cream recalled over manufacturing practice deviations
Med Pride 1% Clotrimazole Antifungal Cream, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 5,755 tubes are affected.
Product
Med Pride, 1% Clotrimazole Antifungal Cream, Net Wt. 1oz (28.3g), Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 524103 0244 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2417-2026·2026-06-24
Medline cath lab and angio packs contain recalled Mastisol adhesive
Medline Minor Cath Lab Packs, OR Vascular Angio Packs and Port-A-Cath kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2443-2026·2026-06-24
Medline Port A Cath kits contain recalled Mastisol liquid adhesive
The Medline Port A Cath convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: PORT A CATH DYNJ906818A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2440-2026·2026-06-24
Medline driveline and port dressing kits contain recalled Mastisol adhesive
The Medline Driveline Management Kit and Port Dressing Change Kit are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2450-2026·2026-06-24
ALYON surgical light head intensity control buttons may detach
ALYON Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 549 units are affected.
Product
ALYON Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2026·2026-06-24
Med Pride bacitracin zinc ointment 500 units recalled over manufacturing deviations
Med Pride Bacitracin Zinc Ointment, 500 units per gram in 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,374 tubes affected.
Product
Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30354 8.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2444-2026·2026-06-24
Medline vascular and cardiac packs contain recalled Mastisol liquid adhesive
Medline convenience kits including AV fistula, endovascular, EP device and aneurysm packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MR
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2424-2026·2026-06-24
Medline basic and laparoscopy packs contain recalled Mastisol liquid adhesive
Medline convenience kits including basic packs, general laparoscopy, CVC insertion bundles and da Vinci packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2026·2026-06-24
Lil Drug Store triple antibiotic ointment recalled over manufacturing deviations
Lil Drug Store Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,225 tubes affected.
Product
Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g), Product distributed by: Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0590-2026·2026-06-24
Kerr Insta-Char aqueous charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char in an aqueous base, 50 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2426-2026·2026-06-24
Medline pediatric dressing change kits contain recalled Mastisol liquid adhesive
The Medline Kit: Dressing Change Ped is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2449-2026·2026-06-24
HarmonyAIR A-Series surgical light intensity control buttons may detach
HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 2,101 units affected.
Product
HarmonyAIR A-Series Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2026·2026-06-24
Lucky Super Soft athlete's foot cream recalled over manufacturing deviations
Lucky Super Soft Antifungal Athlete's Foot Cream, clotrimazole 1%, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,102 tubes affected.
Product
Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0634-2026·2026-06-24
Cura Hongos clotrimazole cream recalled over manufacturing practice deviations
Cura Hongos Crema Antifungica, clotrimazole 1%, in 2 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 84 tubes affected.
Product
Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 52924 00683 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0639-2026·2026-06-24
Med Pride hydrocortisone cream 16oz tubes recalled over manufacturing deviations
Med Pride Hydrocortisone Cream 1%, 16 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,738 tubes are affected.
Product
Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 16oz (454g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 305061.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0589-2026·2026-06-24
Kerr Insta-Char 25 gram aqueous suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char in an aqueous base, 25 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2425-2026·2026-06-24
Medline IV start kits with HubGuard contain recalled Mastisol adhesive
The Medline IV Start Kit with HubGuard is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662
Category
Medical Device
Distribution
Distributed nationwide