State

Rhode Island product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31426–31450 of 76787

HighFDA (Devices)·Z-1051-2020·2020-02-12
Centurion Circumcision Tray Kits Recalled for Incomplete Sterile Seals
Centurion Medical Products is recalling specific Circumcision Tray Kits because incomplete seals on the sterile packaging may compromise sterility.
Product
Centurion- Circumcision Tray Kits DYNDF1078C CIRCUMCISION TRAY DYNDF1082 CIRCUMCISION TRAY DYNDF1082 CIRCUMCISION TRAY DYNDF1093C UNIVERSAL CIRCUMCISION TRAY W/O CLAMP DYNDF1093C UNIVERSAL CIRCUMCISION TRAY W/O CLAMP DYNDF1109 TRAY,CIRCUMCISION DYNDF1128…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2020·2020-02-12
Centurion Medical Products Recalls Dressing Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific dressing trays and medical packs because incomplete seals may compromise sterility.
Product
Centurion- Dressing Tray M101156A DRESSING TRAY M101167A DRESSING TRAY M101168A DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101172B MINOR CORE DRESSING TRAY M101172B MINOR CORE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1056-2020·2020-02-12
Centurion Medical Products Recalls Sterile Biopsy and Arthrogram Trays
Centurion Medical Products is recalling specific sterile biopsy and arthrogram trays due to incomplete seals that may compromise sterility.
Product
Centurion- SPEC0002B ARTHROGRAM TRAY SPEC0002B ARTHROGRAM TRAY SPEC0004C ARTHROGRAM TRAY SPEC0071B CUSTOM BX TRAY SPEC0076G STEREO BIOPSY PACK-LF SPEC0122 BASIC BIOPSY TRAY SPEC0130B BREAST BIOPSY TRAY SPEC0158A CT BIOPSY TRAY SPEC0248B GENERAL BIOPSY TRAY- LF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2020·2020-02-12
Ethicon Recalls VICRYL Sutures Due to Braid Fraying
Ethicon is recalling specific VICRYL sutures because braid fraying may reduce tensile strength. The recall covers 23,688 units distributed in the US and Puerto Rico.
Product
Coated VICRYL (Polyglactin 910) Suture, 18" (45cm) Product Code J497H. The device is a synthetic absorbable sterile surgical suture.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1021-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NONREINF SURG GOWN 3XL BNS, Item Code 9585N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0960-2020·2020-02-12
Cook Inc. Recalls Fixed Core Straight Safety Wire Guide
Cook Inc. is recalling 15 units of Fixed Core Straight Safety Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients.
Product
Fixed Core Straight Safety Wire Guide, Guidewire, Global Product Number G14285
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0969-2020·2020-02-12
Cook Percutaneous Pigtail Nephrostomy Set Recalled for Wire Guide Loading Error
Cook Inc. is recalling Percutaneous Pigtail Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
Product
Percutaneous Pigtail Nephrostomy Set , Global Product No. G14094 G14095 G14899 G14329
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1081-2020·2020-02-12
Centurion Debridement Tray Recalled for Incomplete Sterile Package Seals
Centurion Medical Products Corporation is recalling Debridement Trays because incomplete seals on the sterile package may compromise sterility.
Product
Centurion- I86625 DEBRIDEMENT TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1074-2020·2020-02-12
Centurion Skin Prep Tray Recalled for Incomplete Sterile Package Seals
Centurion Medical Products Corporation is recalling Skin Prep Trays due to incomplete seals on the sterile package, which may compromise sterility.
Product
Centurion-Skin Prep Tray DYNDP1015 SKIN PREP TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2020·2020-02-12
Centurion Medical Recalls Skin Prep Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific lots of sterile skin prep trays because incomplete seals may compromise sterility.
Product
Centurion-Skin Prep Trays SP1180 DRY PREP SET SP200 SKIN SCRUB TRAY SP415 STERILE GAUZE SPONGE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1005-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABREINF SCRUB SURG GWN L NS, Gown. Item Code 90970NA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1094-2020·2020-02-12
Centurion Medical Recalls Umbilical Catheter Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific umbilical catheter trays because incomplete seals on the sterile package may compromise sterility.
Product
Centurion- UVT1045 UMBILICAL ARTERY TRAY UVT1055 UVC KIT UVT1065 UMBILICAL VESSEL CATHETER TRAY UVT170 UMBILICAL VESSEL TRAY W/O CATHETER UVT280 UMBILICAL ARTERY TRAY UVT460 UMBILICAL CATHETER TRAY UVT505 UMBILICAL VESSEL CATH INSERT TR W/O CATH UVT630…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0965-2020·2020-02-12
Cook Inc. Recalls Angled Tip Ureteral Catheter Sets Due to Loading Defect
Cook Inc. is recalling 13,388 Angled Tip Ureteral Catheter Sets because the wire guide may load incorrectly, causing the stiff tip to enter the patient instead of the flexible tip.
Product
Angled Tip Ureteral Catheter Set, Ureteral Catheter, Global Product No. G14598
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1041-2020·2020-02-12
Implant Direct Sybron Recalls Legacy 3 Dental Implants Due to Incorrect Packaging
Implant Direct Sybron is recalling 72 Legacy 3 dental implants because some packages contain incorrect implants, which could lead to surgery rescheduling.
Product
Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0990-2020·2020-02-12
Cardinal Health Recalls Genius 2 Tympanic Thermometers for Accuracy Drift
Cardinal Health is recalling Genius 2 Tympanic Thermometers because calibration frequency may not ensure readings stay within the stated accuracy range.
Product
Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0994-2020·2020-02-12
Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift
Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.
Product
Genius 2 Tympanic Thermometer Private Label Item Code: 3069
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0992-2020·2020-02-12
Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift
Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.
Product
Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0838-2020·2020-02-12
Macleods Pharma Recalls Subpotent Pioglitazone and Metformin Tablets
Macleods Pharma USA is recalling two lots of Pioglitazone and Metformin Hydrochloride tablets because they tested below the required potency levels.
Product
PIOGLITAZONE AND METFORMIN HYDROCHLORIDE — PIOGLITAZONE AND METFORMIN HYDROCHLORIDE (PIOGLITAZONE AND METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0988-2020·2020-02-12
Zimmer Biomet Recalls Jamshidi Bone Marrow Aspiration Needles Due to Labeling Error
Zimmer Biomet is recalling 133 Jamshidi Bone Marrow Aspiration Needles because the outer expiration date may exceed the inner label date.
Product
Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2020·2020-02-12
Teva Recalls Desmopressin Acetate Tablets Due to Missing Desiccant
Teva Pharmaceuticals USA is recalling Desmopressin Acetate Tablets because bottles may be missing desiccant, a GMP deviation.
Product
Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0827-2020·2020-02-12
Ascend Recalls Minocycline Hydrochloride Tablets for Dissolution Failures
Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets due to low dissolution test results.
Product
MINOCYCLINE HYDROCHLORIDE — MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0832-2020·2020-02-12
Graviti Pharmaceuticals Recalls Atorvastatin Calcium Tablets Due to Foreign Tablet Presence
Graviti Pharmaceuticals is recalling 29,056 bottles of 10 mg Atorvastatin Calcium Tablets because a 20 mg tablet was found in a bottle labeled for 10 mg tablets.
Product
Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA; Manufactured By: Graviti Pharmaceuticals Pvt. Ltd., Telangana -502307, INDIA; NDC 70377-027-11.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2020·2020-02-12
Teva Recalls Desmopressin Acetate Tablets Due to Missing Desiccant
Teva Pharmaceuticals USA is recalling Desmopressin Acetate Tablets because bottles may be missing desiccant, a GMP deviation.
Product
Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2465-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0829-2020·2020-02-12
Unichem Recalls Clonidine Hydrochloride Tablets Due to Benzophenone Migration
Unichem Pharmaceuticals is recalling Clonidine Hydrochloride tablets due to potential benzophenone migration from container labels. This is a precautionary measure.
Product
CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V074000·2020-02-11
Blue Bird Recalls 2018-2019 School Buses Due to Wire Harness Defect
Blue Bird is recalling 2018-2019 Vision and All American school buses because a wire harness connector may unplug, causing sudden loss of drive power and power steering.
Product
BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide