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.

3826–3850 of 75983

HighFDA (Devices)·Z-0952-2026·2025-12-24
Chest tube procedure trays recalled over misleading instructions for securing the device
Rocket Medical is recalling 630 Rocket 18Fg Seldinger Catheter Procedure Trays because the instructions and kit labeling contain misleading statements that can lead to improper securing.
Product
Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied w
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-0951-2026·2025-12-24
Twelve French catheters with safety guard recalled over misleading securing instructions
Rocket Medical is recalling 240 Rocket 12Fg Seldinger Catheters with Safety Guard because the instructions and kit labeling contain misleading statements that can lead to improper securing.
Product
Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplie
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-0959-2026·2025-12-24
Leukemia test kits recalled in a second lot family over inaccurate results
Cepheid is recalling 6,325 Xpert BCR-ABL Ultra kits, catalog GXBCRABL-US-10, because specimens with an elevated white blood cell count above 30,000 cells may cause inaccurate results.
Product
Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10
Category
Medical Device
Distribution
29 states
ModerateFDA (Drugs)·D-0228-2026·2025-12-24
Xylocaine dental cartridges recalled over cracked and broken containers
Novocol Pharmaceutical of Canada is recalling 18,789 cartons of 2% Xylocaine Dental with Epinephrine over a defective container with cracked or broken cartridges.
Product
2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose cartridges, 1.7 mL each, Rx only, Manufactured for Dentsply Pharmaceutical, York, PA 17404, by Novocol Pharmaceutical of Canada, Inc., NDC
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0937-2026·2025-12-24
Spinal navigation guide recalled for naming an incompatible toolcard system
SeaSpine Orthopedics is recalling 310 NorthStar OCT Navigation items because the surgical technique guide incorrectly identified Medtronic Infinity toolcards as compatible.
Product
Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-4001
Category
Medical Device
Distribution
24 states
ModerateFDA (Drugs)·D-0240-2026·2025-12-24
Ciclopirox shampoo recalled after failing impurity specifications at eighteen months
Sun Pharma/Taro is recalling 17,664 units of Ciclopirox Shampoo 1% after out of specification impurity and degradation results at the 18-month timepoint.
Product
Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0956-2026·2025-12-24
Children's mouthguards recalled for distribution without FDA premarket clearance
Myofunctional Research Company USA is recalling 436 Myosa for Kids devices because the firm mistakenly distributed the product within the US without FDA premarket clearance or approval.
Product
Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouthguard in 3 different sizes (sm, med, lg) that can be used in children ages 3-15 to address breathing and myofunctional disorders. Catalog Numbers:
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0231-2026·2025-12-24
Mepivacaine dental cartridges recalled over cracked and broken containers
Novocol Pharmaceutical of Canada is recalling 5,520 cartons of Mepivacaine HCl 3% injection over a defective container with cracked or broken cartridges.
Product
MEPIVACAINE — MEPIVACAINE (MEPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0236-2026·2025-12-24
Cisatracurium 10 mg vials recalled after subpotent stability assay results
Somerset Therapeutics is recalling 52,340 vials of Cisatracurium Besylate Injection, 10 mg/5 mL, after out of specification assay results during long term stability testing.
Product
CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0233-2026·2025-12-24
Carbocaine dental cartridges recalled over cracked and broken containers
Novocol Pharmaceutical of Canada is recalling 40 cartons of Cook-Waite Carbocaine 3% mepivacaine injection over a defective container with cracked or broken cartridges.
Product
CARBOCAINE — CARBOCAINE (MEPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0230-2026·2025-12-24
Polocaine dental cartridges recalled over cracked and broken containers
Novocol Pharmaceutical of Canada is recalling 5,825 units of 3% Polocaine Dental mepivacaine injection over a defective container with cracked or broken cartridges.
Product
POLOCAINE — POLOCAINE (MEPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0234-2026·2025-12-24
Phentolamine mesylate injection recalled over cracked and broken cartridges
Novocol Pharmaceutical of Canada is recalling 1,636 cartons of OraVerse (Phentolamine Mesylate) Injection over a defective container with cracked or broken cartridges.
Product
ORAVERSE — ORAVERSE (PHENTOLAMINE MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0229-2026·2025-12-24
Lidocaine and epinephrine dental cartridges recalled over cracked containers
Novocol Pharmaceutical of Canada is recalling 12,033 cartons of Lidocaine HCl 2% with Epinephrine 1:100,000 injection over a defective container with cracked or broken cartridges.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0232-2026·2025-12-24
Benco mepivacaine cartridges recalled over cracked and broken containers
Novocol Pharmaceutical of Canada is recalling Mepivacaine HCl 3% injection distributed by Benco Dental over a defective container with cracked or broken cartridges.
Product
MEPIVACAINE — MEPIVACAINE (MEPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0238-2026·2025-12-24
Cisatracurium 20 mg multiple-dose vials recalled after subpotent assay results
Somerset Therapeutics is recalling 71,310 vials of Cisatracurium Besylate Injection, 20 mg/10 mL, after out of specification assay results during long term stability testing.
Product
CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0237-2026·2025-12-24
Cisatracurium 200 mg vials recalled after subpotent stability assay results
Somerset Therapeutics is recalling 28,660 vials of Cisatracurium Besylate Injection, 200mg/20mL, after out of specification assay results during long term stability testing.
Product
CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0957-2026·2025-12-24
Bone fixation screws recalled over a labeling error on one lot
Smith & Nephew is recalling 168 BIOSURE HA Screws, 6mm x 20mm, due to a labeling error on the affected lot.
Product
BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0931-2026·2025-12-24
Balloon pump instructions updated to reference the correct vibration standards
Datascope is recalling 11,470 Cardiosave Hybrid units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Product
Cardiosave Hybrid
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0932-2026·2025-12-24
Rescue balloon pump instructions updated to reference the correct vibration standards
Datascope is recalling 47 Cardiosave Rescue units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Product
Cardiosave Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V907000·2025-12-23
KTM motorcycle side stand spring may break and fall down
KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.
Product
KTM — KTM 390 ENDURO R, 390 ADVENTURE X, 390 SMC R, 390 ADVENTURE R
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V909000·2025-12-23
Altec Recalls 2022-2023 Aerial Work Platforms Due to Missing Check Valve
Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.
Product
ALTEC — ALTEC AN46, AM55, AA55, AN55
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V906000·2025-12-23
BMW i4 positive battery cable connection may become loose
BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.
Product
BMW — BMW I4 EDRIVE40
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V911000·2025-12-23
Honda CBR650R wiring damage can blow the fuse for lights
Honda is recalling certain 2024-2025 CBR650R motorcycles because engine vibration may damage the turn signal switch wire harness, causing a short circuit and a blown fuse.
Product
HONDA — HONDA CBR650R
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V908000·2025-12-23
Volvo rearview camera image may not display when reversing
Volvo is recalling certain 2021-2025 vehicles across the XC40, XC60, XC90, S60, S90, V60 and V90 ranges because the rearview camera image may not display when the vehicle is in reverse.
Product
VOLVO — VOLVO C40BEV, EC40, EX40, XC90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V905000·2025-12-23
Tiffin motorhome generator wiring harness may contain undersized wires
Tiffin is recalling certain 2025-2026 Open Trail motorhomes fitted with an optional diesel or propane generator because the wiring harness may contain incorrectly sized wires.
Product
TIFFIN — TIFFIN OPEN TRAIL
Category
Vehicle
Distribution
Distributed nationwide