State

Rhode Island product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50451–50475 of 76878

SevereFDA (Drugs)·D-0859-2016·2016-06-01
Teva Recalls Amikacin Sulfate Injection Due to Glass Particulate Matter
Teva Pharmaceuticals USA is recalling Amikacin Sulfate injection vials because glass particulate matter was identified in one vial.
Product
Amikacin Sulfate injection USP,1 gm/4 mL (250 mg/mL) 4mL vial, Rx only, Manufactured in Hungary For: Teva Pharmaceuticals USA, INC. North Wales, PA 19454. Individual Pack NDC 0703-9040-01, Shelf Pack NDC 0703-9040-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1823-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Instruments Due to Seal Defects
Biomet, Inc. is recalling specific trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Screw, fixation, bone.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0866-2016·2016-06-01
Fresenius Kabi Recalls Octreotide Acetate Injection Due to Impurities
Fresenius Kabi is recalling specific lots of Octreotide Acetate Injection because they failed impurities and degradation specifications.
Product
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0902-2016·2016-06-01
FDA Recalls Mojo Risen Distributed Without Approved New Drug Application
R Thomas Marketing, LLC is recalling Mojo Risen capsules nationwide because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Mojo Risen, packaged in BIG BOX (24 individual cards / 2 capsules per card/ 48 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0898-2016·2016-06-01
Happy Passengers Recalled for Lack of FDA Approval
R Thomas Marketing, LLC is recalling Happy Passengers capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Happy Passengers, packaged in BIG BOX (30 small boxes / 1 capsule per box / 30 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·16V392000·2016-06-01
KYMCO Recalls 2016 K-Pipe Motorcycles Due to Reverse Gear Shift Pattern
KYMCO USA is recalling 340 model year 2016 K-Pipe motorcycles because the gear shift pattern was assembled in reverse, which may cause riders to select the wrong gear and increase crash risk.
Product
KYMCO — KYMCO K-PIPE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1821-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Instruments Due to Seal Defects
Biomet is recalling various trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility.
Product
Various trauma and sports medicine instruments and implants. Bit, drill.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling 442 boxes of Delicot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Delicot 10 mm x 13 mm Ref Number: 63-03 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2016·2016-06-01
AngioVac Circuit Packs Recalled for Excessive Endotoxin Levels
AngioDynamics is recalling AngioVac Circuit Packs because they may contain RotaFlow Centrifugal Pumps with endotoxin levels exceeding regulatory limits.
Product
AngioVac Circuit Pack (Tandem Packs), REF/Catalog No. 25-187, UPN H965251870, STERILE, Rx Only, Single Use Only -- The AngioVac Circuit and AngioVac Circuit Pack are designed to be used with the AngioVac Cannula.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 39 boxes of Ultracot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Ultracot 15 mm x 20 mm (Glassine) Ref Number: 23-04G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1829-2016·2016-06-01
RTI Surgical Recalls Streamline OCT Spinal Fixation Instruments
RTI Surgical is recalling 17 Streamline OCT Crosslink Counter Torque Sleeves because a defect may obstruct the cannula, potentially causing driver slippage and patient injury.
Product
Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1753-2016·2016-06-01
American Surgical Cotton Balls Recalled for Packaging Sterility Defect
American Surgical Company is recalling 87 boxes of strung cotton balls due to packaging defects that compromise sterility.
Product
American Surgical Cotton Balls-Strung 1/4" Ref Number: 30-00 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2016·2016-06-01
AngioVac Circuit Recall Due to Potential Endotoxin Levels
Angiodynamics is recalling Vortex MEDICAL AngioVac Circuits because they may contain endotoxin levels exceeding regulatory limits.
Product
Vortex MEDICAL AngioVac Circuit, REF/UPN VTX3100, STERILE, Rx Only, Single Use Only -- The AngioVac Circuit and AngioVac Circuit Pack are designed to be used with the AngioVac Cannula.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1706-2016·2016-06-01
GE Healthcare Discovery IGS 730 Recalled for Potential Image Loss
GE Medical Systems is recalling 54 Discovery IGS 730 systems due to a risk of non-recoverable loss of image acquisition during procedures.
Product
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2016·2016-06-01
American Surgical Ray-Cot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Ray-Cot sponges because defective packaging may compromise sterility. The recall covers 16 boxes distributed worldwide.
Product
American Surgical Ray-Cot 3" x 3" Ref Number: 60-15 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1729-2016·2016-06-01
American Surgical Americot Blue Sponges Recalled for Packaging Defects
American Surgical Company is recalling Americot Blue sponges because defective packaging may compromise sterility. The recall covers 37 boxes distributed worldwide.
Product
American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1806-2016·2016-06-01
American Surgical Telfa Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Telfa 1" x 3" sponges because defective packaging compromises sterility. The recall covers 57 boxes distributed worldwide.
Product
American Surgical Telfa 1" x 3" Ref Number: 80-13 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Implants Due to Seal Defects
Biomet is recalling various trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Plate, fixation, bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1789-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Delicot sponges because defective packaging may compromise sterility. The recall covers 343 boxes distributed worldwide.
Product
American Surgical Delicot 20 mm x 60 mm Ref Number: 63-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2016·2016-06-01
American Surgical Delicot-J Sponges Recalled for Sterility Compromise
American Surgical Company is recalling 68 boxes of Delicot-J sponges because defective packaging compromises sterility. The products were distributed worldwide.
Product
American Surgical Delicot-J 15 mm x 20 mm Ref Number: 63-04J (Japan Only) Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1721-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling 351 boxes of Delicot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Delicot 15mm x 20mm Ref: 63-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2016·2016-06-01
Draeger D-Vapor Anesthesia Vaporizers Recalled for Anesthetic Agent Release
Draeger Medical is recalling D-Vapor and D-Vapor 3000 anesthesia vaporizers because they may release desflurane during filling, posing an eye irritation risk.
Product
Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and Bottles. Catalog # M35500 (D-Vapor) and M36700 (D-Vapor 3000). Anesthesia Vaporizer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling 33 boxes of Ultracot sponges because defective packaging may compromise sterility. The affected products were distributed worldwide.
Product
American Surgical Ultracot 30 mm x 90 mm (Glassine) Ref Number: 23-15G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1799-2016·2016-06-01
American Surgical Cylindrical Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 11 boxes of cylindrical sponges because defective packaging may compromise sterility.
Product
American Surgical Cylindrical Sponges-Strung 1/2" x 1.5" Ref Number: 70-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2016·2016-06-01
American Surgical Policot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Policot sponges because defective packaging compromises sterility. The products were distributed worldwide.
Product
American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide