State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49201–49225 of 76871

HighFDA (Devices)·Z-2328-2016·2016-08-10
Philips IntelliVue Patient Monitor Recall for Outdated Waveform Data
Philips is recalling IntelliVue Patient Monitors because they may display outdated waveform data if powered on continuously for several months, failing to reflect current patient conditions.
Product
IntelliVue Patient Monitor Product Usage: The monitors are indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. The monitors are intended to be used for monitoring and recording of, and to generate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2332-2016·2016-08-10
Stryker Recalls Spirit Select and Plus Hospital Beds Due to Actuator Failure
Stryker Medical is voluntarily recalling Spirit Select and Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Product
Spirit Select Bed, A-C Powered Hospital Bed
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1454-2016·2016-08-10
Isomeric Pharmacy Recalls Betamethasone Injectable Suspension Due to Particle Issues
Isomeric Pharmacy Solution is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension due to potential drug clumps and larger particle sizes.
Product
Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2308-2016·2016-08-10
Beckman Coulter Recalls AU480 Chemistry Analyzers Due to Leaking C Cups
Beckman Coulter is recalling AU480 Chemistry Analyzers because leaking C cups can cause coolant to short-circuit the instrument's circuit boards.
Product
AU480 Chemistry Analyzers, Reference No. B28624 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2310-2016·2016-08-10
Beckman Coulter AU5800 Chemistry Analyzers Recalled for Leaking C Cups
Beckman Coulter is recalling AU5800 Chemistry Analyzers because cracked C cups can leak coolant onto circuit boards, causing short-circuits and instrument stop mode.
Product
AU5800 Chemistry Analyzers, Reference No. A98352 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2337-2016·2016-08-10
Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 90 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2303-2016·2016-08-10
Merge PACS Software Recall for Annotation Display Defect
Merge Healthcare is recalling Merge PACS 6.0 software because it fails to display annotations on certain loaded studies.
Product
Merge PACS software. The firm name on the label is Merge Healthcare, Hartland, Wisconsin. Merge PACS 6.0 is software intended to create and display two-dimensional and three-dimensional images of anatomy from a series of digitally acquired images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2336-2016·2016-08-10
Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 70 units of Air Dermatome II Width Plates because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . Width plates is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2335-2016·2016-08-10
Zimmer Air Dermatome II Handpiece Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 220 Air Dermatome II handpieces because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Handpiece w/o Hose, item number 00-8851-001-01. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2319-2016·2016-08-10
Medtronic StealthStation Software Recalled Due to Scanner Compatibility Issues
Medtronic Navigation is voluntarily recalling 27 units of StealthStation software due to compatibility issues with specific floor-based scanners.
Product
MACH AxiEM Cranial Treon. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2313-2016·2016-08-10
Medtronic Navigation Recalls Synergy Cranial S7 Software Applications
Medtronic Navigation is conducting a voluntary field action for Synergy Cranial S7 software applications due to compatibility issues with specific floor-based scanners.
Product
Synergy Cranial S7. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2304-2016·2016-08-10
Roche Recalls Vancomycin Assay Kits Due to Incorrect Method Sheets
Roche Diagnostics is voluntarily recalling Vancomycin assay kits because method sheets contain incorrect comparison data for specific analyzers.
Product
ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin (917, MOD P) The ONLINE TDM Vancomycin assay is for the quantitative determination of Vancomycin in human serum or plasma on Roche automated clinical chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2316-2016·2016-08-10
Medtronic Navigation StealthStation Software Voluntary Field Action
Medtronic Navigation is conducting a voluntary field action for StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Product
Synergy Spine. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2338-2016·2016-08-10
Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 60 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2326-2016·2016-08-10
Mentor MemoryGel Breast Implant Recall Due to Missing Date Labels
Mentor Texas, LP is recalling 35 units of 300cc MemoryGel Breast Implants because the boxes were labeled with null manufacturing and expiration dates.
Product
Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction.
Category
Medical Device
Distribution
11 states
ModerateFDA (Devices)·Z-2334-2016·2016-08-10
Zimmer Air Dermatome II Handpieces Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 630 Air Dermatome II handpieces because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2317-2016·2016-08-10
Medtronic Navigation Recalls Fusion ENT Software Application
Medtronic Navigation is voluntarily recalling 27 units of the Fusion ENT software application due to a field action involving Neurologica scanners.
Product
Fusion ENT Application. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2302-2016·2016-08-10
Ortho-Clinical Diagnostics Recalls VITROS Total T4 Reagent Packs
Ortho-Clinical Diagnostics is recalling VITROS Total T4 Reagent Packs because test results may show a negative bias before the 8-week storage limit.
Product
VITROS Immunodiagnostic Products Total T4 Reagent Pack, REF/Product Code 874 4468, Unique Identifier No. 10758750005147, IVD --- Ortho-Clinical Diagnostics, For in vitro diagnostic use only. For the quantitative measurement of total thyroxine (T4) in human serum and plasma…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2318-2016·2016-08-10
Medtronic Navigation Recalls StealthStation Software Applications
Medtronic Navigation is voluntarily recalling StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Product
MACH Cranial Treon. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2340-2016·2016-08-10
Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects
Zimmer Surgical Inc is recalling 110 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.
Product
Zimmer¿ Air Dermatome II Width Plate, 4 inch. Part #00-8851-204-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2314-2016·2016-08-10
Medtronic Navigation Recalls StealthStation Software Applications
Medtronic Navigation is conducting a voluntary field action for StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Product
FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2315-2016·2016-08-10
Medtronic Navigation Recalls S7 MACH FrameLink Software Applications
Medtronic Navigation is conducting a voluntary field action for S7 MACH FrameLink software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Product
S7 MACH FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2309-2016·2016-08-10
Beckman Coulter AU680 Chemistry Analyzers Recalled for Leaking C Cups
Beckman Coulter is recalling AU680 Chemistry Analyzers because leaking and cracked C cups can cause coolant to leak onto circuit boards, resulting in short-circuits and instrument stop mode.
Product
AU680 Chemistry Analyzers, Reference No. B04779 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1453-2016·2016-08-10
Teva Recalls Children's Qnasl Nasal Aerosol for Content Uniformity Failure
Teva North America is recalling Children's Qnasl nasal aerosol canisters due to failed spray content uniformity tests. The FDA classified this as a Class III recall.
Product
Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2333-2016·2016-08-10
C.R. Bard Recalls SureStep Urine Collection System for Labeling Issues
C.R. Bard is recalling 530 SureStep urine collection systems due to a labeling problem. The recall is voluntary and nationwide.
Product
SureStep Tray, with Add-a-Foley, COMPLETE CARE, Drainage Bag, and STATLOCK Stabilization The product is a urine collection system that includes a STATLOCK Foley Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide