State

Rhode Island product recalls

73,100 recalls have nationwide distribution and so reach Rhode Island. 3,046 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,046
Critical: 221
Severe: 572
Most recent: 2026-09-23

Of the 3,046 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 572 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,046 recalls whose distribution notice names Rhode Island specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10751–10775 of 76146

SevereFDA (Devices)·Z-2251-2024·2024-07-17
Bausch+Lomb I-PACK Injection Kit Recalled for Unvalidated Sterilization
Synergetics Inc is recalling the Bausch+Lomb I-PACK Injection Kit nationwide because sterilization certificates could not be validated by the supplier. The unvalidated sterilization of this eye injection device poses a potential infection risk.
Product
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0588-2024·2024-07-17
OTC Sunscreen Foundation Recalled for Fungal Mold Contamination
Suntegrity IMPECCABLE SKIN sunscreen foundation is recalled for microbial contamination with Aspergillus Sydowii mold. Consumers should discontinue use immediately.
Product
IMPECCABLE SKIN - IVORY — IMPECCABLE SKIN - IVORY (ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2253-2024·2024-07-17
BAUSCH+LOMB I-PACK Injection Kit Recalled Due to Sterilization Validation Failure
FDA has recalled 116 units of BAUSCH+LOMB I-PACK Injection Kits because sterilization certificates could not be validated by the supplier, creating potential infection risk for patients receiving intravitreal eye injections.
Product
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2254-2024·2024-07-17
Intravitreal Injection Kit Recalled for Unvalidated Sterilization Certificates
Synergetics Inc is recalling 35 units of the BAUSCH+LOMB I-PACK Intravitreal Injection Kit because sterilization certificates could not be validated, creating an infection risk.
Product
BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2024·2024-07-17
Hemodialysis System Blood Pump Rotor Recall Due to Loose Sheaves
Fresenius is recalling blood pump rotors in home hemodialysis systems due to loose or dislodged guide sheaves reported during clinical use. The defect could affect proper pump operation during dialysis treatment.
Product
RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2285-2024·2024-07-17
Foot-Ankle Procedure Tray Recalled for Excessive Sterilization Residue
American Contract Systems Inc is recalling 107 units of FOOT ANKLE-LF Procedure tray distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits for permanent-implant devices.
Product
FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1470-2024·2024-07-17
C. Kreuger Gluten Free Peanut Butter Cookies recalled for missing ingredient statement
C. Krueger Finest Baked Goods is recalling C. Kreuger Gluten Free Peanut Butter Cookies due to missing ingredient statement on labels, preventing consumers from identifying allergens. The recall affects 4,538 cookies distributed across all U.S. states.
Product
C. Kreuger Gluten Free Peanut Butter Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for 30 days at ambient and 1 year frozen.
Category
Food
Distribution
50 states
HighFDA (Drugs)·D-0587-2024·2024-07-17
Dianeal Low Calcium Dialysis Solution Recall: Sterility Risk from Connector Leaks
Baxter Healthcare recalls 6,874 bags of Dianeal Low Calcium peritoneal dialysis solution due to potential leaks in the connector assembly that could compromise product sterility.
Product
DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2024·2024-07-17
Knee Procedure Kit Recalled for Elevated Chemical Residuals
American Contract Systems Inc is recalling 26 TOTAL KNEE Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residues on the cast padding component that exceed safe exposure limits.
Product
TOTAL KNEE -Procedure Kit Catalog Number: QPTK95B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1469-2024·2024-07-17
Gluten Free Cookies Recalled for Missing Ingredient Statement on Label
C. Krueger Finest Baked Goods is recalling 3,347 Gluten Free White Chocolate Cherry Oatmeal Cookies due to missing ingredient statements on labels, preventing consumers from identifying allergens and dietary content.
Product
C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for 30 days at ambient and 1 year frozen.
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-2309-2024·2024-07-17
Orthopedic ORIF Hip Rod Procedure Kit Recalled for Sterilization Residuals
American Contract Systems Inc is recalling its ORIF HIP IM RODDING FEMUR-Procedure Kit (28 units) because ethylene oxide and ethylene chlorohydrin residuals in the cast padding exceeded safe limits for permanent implants.
Product
ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2024·2024-07-17
Presource surgical kits recalled for syringe design defect risk
Cardinal Health is recalling 136,753 Presource surgical kits nationwide because included Shenli syringes contain design modifications that could cause inaccurate dosing and device leakage, risking patient harm.
Product
Presource kits and trays, labeled as: 1) ANGIOGRAPHY PACK, Catalog Number SAN13BS605; 2) ANGIOGRAPHY PACK, Catalog Number SAN13BS606; 3) ANGIOGRAPHY PACK, Catalog Number SAN13BS607; 4) ANGIOGRAPHY PACK, Catalog Number SAN13BS608; 5) ANGIOGRAPHY PACK, Catalog Number SAN13BS6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0590-2024·2024-07-17
Bupropion Extended-Release Tablets Recalled for Dissolution Failure
Amerisource Health Services is recalling Bupropion Hydrochloride 150mg extended-release tablets nationwide due to dissolution specification failures. The tablets dissolve faster than specified limits.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2329-2024·2024-07-17
Cardiovascular Procedure Kits Recalled for Potential Syringe Design Defects
Cardinal Health recalls 17,445 cardiovascular procedure kits nationwide containing potentially defective syringes that could cause inaccurate dosing or device leakage.
Product
Presource kits and trays, labeled as: 1) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC3; 2) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC4; 3) Cardiovascular Procedure Kit, Catalog Number SAN29ANCCL; 4) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2342-2024·2024-07-17
Blood Pump Rotor Spare Part Recalled for Loose Guide Sheaves
Fresenius Medical Care recalls a blood pump rotor spare part used in dialysis systems in Canada due to reports of loose or dislodged guide sheaves after use. No injuries have been reported.
Product
191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2305-2024·2024-07-17
Hip Procedure Kit Recalled for Excessive Ethylene Oxide Sterilization Residuals
American Contract Systems Inc is recalling 393 units of the TPK Anterior Hip Pack nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe limits for permanent exposure medical devices.
Product
TPK ANTERIOR HIP PACK 176483-Procedure Kit Catalog Number: TPAH21E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2024·2024-07-17
Arthroscopy Kit Recalled for Excessive Sterilant Residue on Padding
American Contract Systems is recalling 27 arthroscopy procedure kits because the cast padding component contains ethylene oxide and ethylene chlorohydrin residues exceeding safe limits for permanent exposure devices.
Product
ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2297-2024·2024-07-17
Total Knee Procedure Kit Recalled for Excess Ethylene Oxide Residue
American Contract Systems Inc is recalling a knee surgery procedure kit (24 units, Lot 939241) due to ethylene oxide sterilization residues in the cast padding exceeding safety exposure limits for permanent-implant devices.
Product
TOTAL KNEE - 297835 -Procedure Kit Catalog Number: RGTK10L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2024·2024-07-17
Knee Arthroscopy Kit Recalled for Elevated Sterilization Chemical Residues
American Contract Systems Inc is recalling 60 units of the KNEE ARTHROSCOPY PACK-Procedure Kit nationwide due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding established safety limits.
Product
KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0594-2024·2024-07-17
Compounded Lidocaine-Epinephrine Injectable Recalled Nationwide for Subpotent Epinephrine
Tailstorm Health Inc is recalling a compounded lidocaine-epinephrine injection nationwide due to subpotent epinephrine component. The recall affects 12,525 vials of lot number 2311003.
Product
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2324-2024·2024-07-17
ZOLL Powerheart G5 AED shipping film may prevent shock delivery
ZOLL Powerheart G5 AED devices are shipped with a protective film on the front panel. If not removed before use, the film may prevent the shock button from being pressed, delaying or preventing defibrillation therapy.
Product
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). Model/Catalog Number: G5S-00A G5S-0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2024·2024-07-17
Procedure Kit Recalled for Excess Ethylene Oxide Residue in Cast Padding
American Contract Systems Inc is recalling 36 units of Hand Pack procedure kits due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding regulatory limits.
Product
HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2281-2024·2024-07-17
Arthroscopy Procedure Tray Recalled for Sterilant Residual Contamination
American Contract Systems Inc is recalling 272 units of the ARTHROSCOPY SUP JOI PACK Procedure Tray because sterilant residuals in the cast padding exceeded safe limits for permanent implant use.
Product
ARTHROSCOPY SUP JOI PACK Procedure tray Catalog Number: BPAS17C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2310-2024·2024-07-17
Hand Procedure Kit Recalled for Excess Ethylene Oxide Residuals
American Contract Systems recalls HAND PACK-Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residuals on the cast padding component, exceeding safe permanent-contact exposure limits.
Product
HAND PACK-Procedure Kit Catalog Number: WEHD16B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2276-2024·2024-07-17
American Contract Systems Surgical Trays Recalled for Ethylene Oxide Residuals
American Contract Systems is recalling MAJOR KNEE surgical procedure trays due to excessive ethylene oxide and ethylene chlorohydrin residuals from sterilization that exceed safety limits for permanent exposure devices.
Product
MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B
Category
Medical Device
Distribution
Distributed nationwide