State

Rhode Island product recalls

73,827 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,054
Critical: 221
Severe: 708
Most recent: 2026-11-04

Of the 3,054 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 708 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54376–54400 of 76881

HighFDA (Devices)·Z-2758-2015·2015-09-16
Intuitive Surgical Recalls Fenestrated Bipolar Forceps for da Vinci System
Intuitive Surgical is recalling 21,684 Fenestrated Bipolar Forceps used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.
Product
Fenestrated Bipolar Forceps; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428093-12, 428093-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V575000·2015-09-16
Vermeer Recalls Brush Chippers and Stump Cutters for Missing Reflectors
Vermeer is recalling specific brush chippers and stump cutters because their LED side marker lights lack required reflectors, reducing vehicle visibility.
Product
VERMEER — VERMEER BC600XL, BC900XL, SC802, BC1000XL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2753-2015·2015-09-16
Intuitive Surgical Recalls da Vinci Si Single-Site Needle Drivers
Intuitive Surgical is recalling 89 da Vinci Si Single-Site Needle Drivers because the jaws may become fixed in a closed position.
Product
Needle Driver; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428056-12, 428056-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2757-2015·2015-09-16
Intuitive Surgical Recalls Curved Needle Drivers for da Vinci System
Intuitive Surgical is recalling 3,698 Curved Needle Drivers used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.
Product
Curved Needle Driver; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428088-12, 428088-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2751-2015·2015-09-16
Intuitive Surgical Recalls da Vinci Si Single-Site Clip Appliers
Intuitive Surgical is recalling 17,617 da Vinci Si Single-Site Clip Appliers because the jaws may become fixed in a closed position during use.
Product
Medium -Large Clip Applier; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428053-12, 428053-15. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15244·2015-09-16
Bradshaw Recalls Jumbo Roasters Due to Sharp Edge Laceration Hazard
Bradshaw International is recalling Good Cook Jumbo Roasters because incorrectly finished rims have sharp edges that can cause cuts.
Product
Roasting pan
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2745-2015·2015-09-16
Smith & Nephew Birmingham Hip Resurfacing Femoral Head Recall
Smith & Nephew is recalling 5,987 units of the Birmingham Hip Resurfacing Femoral Head due to revision rates higher than established benchmarks.
Product
Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD, STERILE R, Rx only, REF Numbers: 74121138 (38 MM), 74123140 (40 MM), 74121142 (42 MM), 74123144 (44 MM), 74121146 (46 MM). Product Usage: Hip joint prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2741-2015·2015-09-16
Siemens Recalls Dimension CREA Tests for Falsely Depressed Results
Siemens Healthcare Diagnostics is recalling Dimension CREA and Dimension Vista CREA tests because they may produce falsely depressed creatinine results in the presence of hemolysis.
Product
Dimension¿ CREA (Creatinine) and Dimension Vista¿ CREA (Creatinine); The CREA method used on the Dimension¿ clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of creatinine in human serum, plasma and urine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2747-2015·2015-09-16
Smith & Nephew Birmingham Hip Resurfacing Dysplasia Cup Recall
Smith & Nephew is recalling Birmingham Hip Resurfacing Dysplasia Cups because the system showed higher revision rates than established benchmarks.
Product
Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR, REF Numbers: 74120246 (46 MM), 74122248 (48 MM), 74120250 (50 MM), 74122252 (52 MM), 74120254 (54 MM) Product Usage: Hip joint prosthesis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2755-2015·2015-09-16
Intuitive Surgical Recalls da Vinci Si Single-Site Crocodile Graspers
Intuitive Surgical is recalling 15,834 da Vinci Si Single-Site Crocodile Graspers because the instrument jaws may become fixed in a closed position.
Product
Crocodile Grasper; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428059-12, 428059-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2756-2015·2015-09-16
Intuitive Surgical Recalls da Vinci Si Maryland Bipolar Forceps
Intuitive Surgical is recalling 13,644 Maryland Bipolar Forceps used with the da Vinci Si Surgical System because the instrument jaws may become fixed in a closed position.
Product
Maryland Bipolar Forceps; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428080-04, 428080-05. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1420-2015·2015-09-16
Mutual Pharmaceutical Recalls Felodipine Tablets Due to Chemical Contamination
Mutual Pharmaceutical is recalling specific lots of Felodipine Extended-Release Tablets because benzophenone leached from the label varnish.
Product
Felodipine Extended-Release Tablets, 2.5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-368-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1427-2015·2015-09-16
Healthpoint Recalls Surgicept Surgical Hand Scrub Due to Chemical Contamination
Healthpoint, Ltd is recalling 11,910 bottles of Surgicept surgical hand scrub because a naphthalene compound was identified in the product.
Product
Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Healthcare Personnel Handwash in 1150 mL bottles. MARKETED BY: CafeFusion, Leawood, KS 66211, MANUFACTURED FOR: HEALTHPOINT, LTD Ft. Worth, Texas 76107, MANUFACTURED BY: DPT LABORATORIES, LTD 3300 Research Plaza…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2740-2015·2015-09-16
DermaPen Pro Micro Needling System Recalled for Lack of FDA Clearance
Derma Pen, LLC is recalling DermaPen Pro Micro Needling Systems because the devices were distributed without FDA clearance or approval.
Product
DermaPen Pro Model, Micro Needling System, a motorized AC powered surgical instrument for dermabrasive use. Each motorized handpiece is packaged within a small box. Each disposable needle cartridge is packaged individually and then placed into boxes of 30 quantities per box.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2744-2015·2015-09-16
Biomet C-Tek Maxan Anterior Cervical Plate System Mislabeled Recall
Biomet Spine is recalling 7 parts of the C-Tek Maxan Anterior Cervical Plate System because some units were mislabeled with an incorrect part number.
Product
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1425-2015·2015-09-16
Mutual Pharmaceutical Recalls Imipramine HCl Tablets Due to Chemical Contamination
Mutual Pharmaceutical is recalling Imipramine HCl tablets because benzophenone leached from the label varnish. The recall covers 10,080 bottles distributed nationwide.
Product
Imipramine HCl Tablets, USP, 50 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-914-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1423-2015·2015-09-16
Mutual Pharmaceutical Recalls Imipramine HCl Tablets Due to Benzophenone Contamination
Mutual Pharmaceutical is recalling 5,472 bottles of Imipramine HCl 10 mg tablets because benzophenone leached from the label varnish.
Product
Imipramine HCl Tablets, USP, 10 mg, 100 count bottles, Rx only, Mfd By: Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 54738-912-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2739-2015·2015-09-16
Siemens ADVIA Centaur Folate Diluent Recalled for Low Recovery Results
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Folate Ascorbic Acid Diluent because it causes low red blood cell control recoveries and low patient sample results.
Product
ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent; SMN 10316877. Used to prepare the Red Blood Cell hemolysate for use with the ADVIA Centaur systems folate assay.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2736-2015·2015-09-16
Medtronic Perfusion Tubing Packs Recalled for Low Ultrafiltration Performance
Medtronic is recalling specific perfusion tubing packs and hemoconcentrators because they demonstrate low ultrafiltration performance below product specifications.
Product
MEDTRONIC PERFUSION TUBING PACKS (with potentially affected Hemoconcentrators). Model # 7U65R2, 8C72R4, 6N21R2, BB7M38R11, TL2Q68R17, HY8R66R3, HY2U43R9, 8C72R4, BB5J59R19, 6B65R3, TL7M46R7, TL2Q68R17, 7U65R2, M074704B, M230002A, BB7M38Rll, M450013B, BB8N86R4, HY2U43R9…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2759-2015·2015-09-16
Biomet Spine Lineum OCC Starter Flexible Instruments Recalled for Design Control Issues
Biomet Spine is recalling Lineum OCC Starter Flexible instruments because they were distributed before design control activities were completed.
Product
Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft, Model Numbers 14-525050 and 14-525057, reusable devices distributed with bubble wrap inside a plastic pouch. The Lineum system is designed to facilitate reconstruction of the cervical and upper thoracic…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1421-2015·2015-09-16
Mutual Pharmaceutical Recalls Felodipine Tablets Due to Chemical Contamination
Mutual Pharmaceutical is recalling specific lots of Felodipine Extended-Release Tablets because benzophenone leached from the product label varnish.
Product
Felodipine Extended-Release Tablets, 5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-369-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1422-2015·2015-09-16
Mutual Pharmaceutical Recalls Felodipine Tablets Due to Chemical Contamination
Mutual Pharmaceutical is recalling specific lots of Felodipine Extended-Release Tablets because benzophenone leached from the label varnish.
Product
Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1424-2015·2015-09-16
Mutual Pharmaceutical Recalls Imipramine HCl Tablets Due to Chemical Contamination
Mutual Pharmaceutical is recalling specific lots of Imipramine HCl tablets because benzophenone leached from the label varnish.
Product
Imipramine HCl Tablets, USP, 25 mg, 100 count bottles, Mfd By: Mutual Pharmaceutical Co., Inc., Philadelphia, PA --- NDC 54738-913-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1419-2015·2015-09-16
CVS Sugar Free Black Cherry Cough Drops Recalled for Foreign Tablets
Bestco, Inc. is recalling CVS Sugar Free Black Cherry Cough Drops because they may contain comingled Sugar Free Honey Lemon cough drops.
Product
CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT), Packaged in a) 25 Drop Bags (UPC: 050428 448526) and b) 36 drop bags (UPC: 050428 476581), Over the Counter. Distributed by: CVS Pharmacy, Inc., One CVS Drive Woonsocket, RI 02895.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V574000·2015-09-15
Honda Recalls 2014-2015 Civic and Fit for Transmission Software Defect
Honda is recalling 2014-2015 Civic and 2015 Fit vehicles to update transmission software that may damage the drive pulley shaft, potentially causing loss of acceleration or wheel lockup.
Product
HONDA — HONDA FIT, CIVIC
Category
Vehicle
Distribution
Distributed nationwide