State

Rhode Island product recalls

73,722 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,053
Critical: 221
Severe: 707
Most recent: 2026-10-28

Of the 3,053 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 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30951–30975 of 76775

HighFDA (Devices)·Z-1352-2020·2020-03-04
Breas Medical Recalls Vivo Ventilator Protective Covers Due to Obstruction Risk
Breas Medical is recalling 629 Vivo ventilator protective covers because the design may obstruct the exhalation valve control pressure tube.
Product
Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the Vivo 50 and Vivo 65 ventilators - Product Usage: The protective cover is intended for additional protection of the Vivo 50, Vivo 55, Vivo 60 and Vivo 65…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1370-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 4MM(H) Reference Number: IEHA354
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1378-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 3MM(H) Reference Number: IEHA463
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1376-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i, LLC is recalling specific lots of Bellatek Encode Healing Abutments because they may produce incorrect rotation or margin contour misalignment in scanned data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 4MM(H) Reference Number: IEHA454
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0791-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling 7,388 cases of Grain Free Granola (Chocolate Fix) because it may be contaminated with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; Chocolate Fix; packaged in 10oz stand-up pouches; UPC 013964497113
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1377-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 6MM(H) Reference Number: IEHA456
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0792-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling 7,388 cases of Grain Free Granola; Apple Pie due to potential contamination with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; Apple Pie; packaged in 10oz stand-up pouches; UPC 013964497106
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1375-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 3MM(H) Reference Number: IEHA453
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0788-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling 7,388 cases of Grain Free Granola due to potential contamination with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; The Original; packaged in 10oz stand-up pouches; UPC 013964497144
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1380-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA466
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1367-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Misalignment
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Product
CERTAIN¿ BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H) Reference Number: IEHA344
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1368-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 6MM(H) Reference Number: IEHA346
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1364-2020·2020-03-04
Exactech Recalls Truliant Splined Stem Extensions Due to Labeling Error
Exactech is recalling four Truliant Splined Stem Extensions because the labels incorrectly identify the implant size as 17mm x 80mm instead of 18mm x 120mm.
Product
Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1386-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in scanned data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1385-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in scanned data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0790-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling Paleonola Grain Free Granola in Pina Colada flavor due to potential contamination with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; Pina Colada; packaged in 10oz stand-up pouches; UPC 091037367808
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1388-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in dental impressions.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 7.5MM(P) X 4MM(H) Reference Number: IEHA574
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1371-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Misalignment
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin contour misalignment in dental impressions.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 6MM(H) Reference Number: IEHA356
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1387-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA566
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0793-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling 7,388 cases of Grain Free Granola; Pumpkin Pie due to potential contamination with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; Pumpkin Pie; packaged in 10oz stand-up pouches; UPC 013964497137
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1379-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because the resulting impression or scanned data may cause incorrect rotation and margin contour misalignment.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA464
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2020·2020-03-04
Randox RX Daytona Plus Clinical Chemistry Analyzer Software Recall
Randox Laboratories is recalling RX Daytona Plus clinical chemistry analyzers to fix software issues causing incorrect sample ordering and quality control flags.
Product
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0789-2020·2020-03-04
Paleonola Grain Free Granola Recalled for Unapproved Herbicide Contamination
Paleonola Llc is recalling Grain Free Granola and Maple Pancake products due to potential contamination with the unapproved herbicide haloxyfop.
Product
Paleonola Grain Free Granola; Maple Pancake; packaged in 10oz stand-up pouches; UPC 013964497120
Category
Food
Distribution
5 states
ModerateFDA (Devices)·Z-1363-2020·2020-03-04
Siemens ADVIA Chemistry Lipase Recalled for Calibration Failures
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Lipase reagents due to customer complaints about failed calibrations and increased imprecision in quality control and patient samples.
Product
ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product Usage: Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas, such as acute pancreatitis and obstruction of the pancreatic duct.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1382-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 3MM(H) Reference Number: IEHA553
Category
Medical Device
Distribution
Distributed nationwide