State

Rhode Island product recalls

73,388 recalls have nationwide distribution and so reach Rhode Island. 3,047 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,047
Critical: 221
Severe: 707
Most recent: 2026-09-30

Of the 3,047 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 3,047 recalls whose distribution notice names Rhode Island specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19276–19300 of 76435

ModerateFDA (Devices)·Z-1792-2022·2022-10-05
Sterilization Chemical Indicator Strips Recalled for Temperature Exposure
Mckesson Medical-Surgical is recalling SPS Medical sterilization indicator strips due to temperature excursions that may have reduced their effectiveness. Products distributed June–September 2021 are affected.
Product
a. SPS MEDICAL SUPPLY Steam Indicator Strip SPSmedical Sterilization Chemical Indicator Strip Steam 4 Inch Model Number: SIS-250. b. SPS MEDICAL SUPPLY SteamPlus Sterilization Integrator Sterilization Steam Plus Monitor Model Number: SSI-1000.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1797-2022·2022-10-05
StayFIX Percutaneous Catheter Fixation Device Recalled Due to Storage Temperature Exposure
MERIT MEDICAL SYSTEMS StayFIX catheter fixation devices recalled due to facility temperature excursions during storage before delivery. Approximately 109 units received between June-September 2021; manufacturer states no adverse health consequences are likely.
Product
MERIT MEDICAL SYSTEMS StayFIX FIXATION DEVICE, STAYFIX F/PERCUTAN CATH 5FR-14FR Model Number: 884450023358. Used to secure anaesthesia catheter.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0005-2023·2022-10-05
Prescription Drug Esomeprazole Out of Specification for Potency
Sun Pharmaceutical is recalling Esomeprazole Magnesium capsules nationwide because the drug potency exceeds the specified level at the 12-month timepoint.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1787-2022·2022-10-05
Saline wound flush recalled due to temperature exposure affecting effectiveness
Mckesson is recalling SafeWash Saline Wound Flush due to temperature exposure that may have reduced product effectiveness. The recall affects units distributed nationwide from June through September 2021.
Product
DERMARITE INDUSTRIES SafeWash Saline Saline Wound Flush SafeWash 7.1 oz. Can Sterile 0.9% Sodium Chloride Model Number: 00245
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1791-2022·2022-10-05
Sterilization Roll Recalled Due to Temperature Exposure During Manufacturing
SPS Medical Supply Crosstex sterilization rolls (model SCT3) are being recalled because they were exposed to high temperatures during manufacturing facility storage before shipment. Temperature exposure may have compromised the product's sterilization effectiveness.
Product
SPS MEDICAL SUPPLY Crosstex International Sterilization Roll Sani-Roll Ethylene Oxide (EO) Gas / Steam 3 Inch X 100 Foot Transparent / Blue Self Seal Paper / Film Model Number: SCT3.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1800-2022·2022-10-05
Wound Care Dressings Recalled Due to Temperature Exposure
Mckesson is recalling Shur-Conform and ALGICELL wound care dressings due to temperature exposure affecting product effectiveness. All affected units were distributed June through September 2021.
Product
a. INTEGRA LIFESCIENCE (WND CARE) Shur-Conform Oil Emulsion Oil Emulsion Impregnated Dressing Shur-Conform 3 X 8 Inch Knitted Cellulose Acetate Petrolatum Emulsion Sterile Model Number: 77042. b. INTEGRA LIFESCIENCE (WND CARE) ALGICELL Ag Silver Alginate Dressing Algicell…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0004-2023·2022-10-05
Esomeprazole Magnesium Capsules Recalled for Out-of-Specification Potency
Sun Pharmaceutical is recalling Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg nationwide due to superpotency findings. Lot AC14299 (expiration 12/2022) tested out of specification for drug assay at the 12-month stability timepoint.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1793-2022·2022-10-05
STERIS Sterilization Indicators Recalled Due to Temperature Excursions
Six sterilization monitoring devices from STERIS Corporation were recalled due to temperature excursions during storage and delivery that may have compromised their effectiveness. Affected products were distributed nationwide between June and September 2021.
Product
a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model Number: LCB053. b. STERIS CORP VERIFY Verify SixCess Sterilization Flash Indicator Strip Steam 2-3/4 Inch Model Number: PCC006. c. STERIS CORP VERIFY Verify Sterilization…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1789-2022·2022-10-05
Collagen Powder Recalled Due to Temperature Exposure During Shipment
DermaCol 100 Collagen Powder was exposed to higher temperatures during storage from June to August 2021. The product's effectiveness may have been impacted, though the FDA determined no adverse health consequences are likely.
Product
DERMARITE INDUSTRIES DermaCol 100 Collagen Powder DermaCol 100 Collagen 1 Gram Model Number: 00300E
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1542-2022·2022-10-05
Ampicillin for Injection Recalled Due to Foreign Object Contamination
Viatris Inc recalls 3,931 cartons of Ampicillin for Injection after a complaint of a hair strand found in one vial. No illnesses have been reported.
Product
Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103 U.S.A
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1790-2022·2022-10-05
SporView Sterilization Biological Indicator Kit Recalled for Temperature Exposure
McKesson is recalling SporView Culture Set biological indicator kits (models CS-020 and CS-100) due to facility temperature excursions that may have compromised product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
a. SporView Culture Set SporView Sterilization Biological Indicator Kit Steam / EO Gas / Dry Heat / Chemical Vapor Model Number: CS-020 b. SPORVIEW CULTURE SET SporView Sterilization Biological Indicator Kit Steam / EO Gas / Dry Heat / Chemical Vapor Model Number: CS-100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1805-2022·2022-10-05
McKesson Calcium Alginate Wound Dressings Recalled for Temperature Exposure During Storage
McKesson Medical-Surgical is recalling multiple calcium alginate wound dressings due to facility temperature excursions that may have impacted product effectiveness. The FDA states the affected products are not likely to cause adverse health consequences.
Product
a. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, CALCIUM ALGINATE SHEET 4"X8" (5/BX 10BX/CS), Catalog #3563. b. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, CALCIUM ALGINATE AG2X2" (10/BX 10BX/CS) Catalog #3557. c. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, CALCIUM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1799-2022·2022-10-05
Surgitube Surgical Bandages Recalled for Temperature Exposure During Storage
McKesson is recalling Surgitube surgical bandages distributed between June and September 2021 that may have been exposed to elevated temperatures during storage. The FDA states the temperature exposure is unlikely to cause adverse health effects.
Product
a. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ15/8" 50YDS Catalog #GL-219. b. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ2 1" 50YDS Catalog # GL-220. c. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ4 25/8" 50YDS Catalog # GL-222. d.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1817-2022·2022-10-05
Starling Monitor Devices Recalled for Incorrect Device Identification Labeling
Baxter Healthcare is recalling Starling Monitor devices and accessories due to incorrect Unique Device Identification (UDI) information on labels and non-compliant barcodes. Approximately 9,671 units distributed nationwide are affected.
Product
Starling Monitor, Product code CMMST5 and Starling Monitor SV, Product code CMM-ST5 (same products); and accessories/spare parts Starling Battery Pack, Product Code CMABATT; and Starling Patient Cable, Product code CMASC10.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1807-2022·2022-10-05
Wound Dressing Units Recalled Due to Storage Temperature Excursions
KerraCel Ag wound dressing units distributed between June and September 2021 are being recalled due to facility temperature excursions that may have affected product effectiveness. The FDA states no adverse health consequences are likely.
Product
3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1806-2022·2022-10-05
McKesson Wound Dressing Products Recalled for Temperature Exposure
McKesson wound dressing products distributed nationwide are being recalled due to exposure to elevated temperatures during storage that may have reduced their effectiveness. No adverse health consequences have been reported.
Product
a. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WOUND GELLING FIBERHIGH-ABSRB 4"X4 3/4" (10/BX) Catalog #87400. b. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WND GELLING FIBER HIABSRB AG 4X4.75 (10/BX 10BX/CS Catalog #177400. c. ADVANCED MEDICAL SOLUTIONS McKesson…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1851-2022·2022-10-05
Leica Surgical Microscopes: Photodiode Defect Causes Inaccurate Illumination
Leica Microsystems is recalling 32 surgical operating microscopes due to a photodiode component defect that produces inaccurate illumination adjustment when BrightCare Plus with Luxmeter is used.
Product
Leica Surgical Operating Microscopes, PROvido Part Numbers: a. 10448976, b. 10448950
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1802-2022·2022-10-05
Medical Monofilament Testing Devices Recalled for Temperature Excursion
Mckesson Medical-Surgical is recalling monofilament sensory testing devices (13 units) due to temperature excursions during June-August 2021. Heat exposure may have compromised device effectiveness.
Product
Medical Monofilament Manufacturing MONOFILIMENT TEST, SENSORY F/FOOT 10GM (40/PK) Model Number: AM140
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1798-2022·2022-10-05
AquaGuard Wound Dressing Recall Due to Facility Temperature Excursions
TIDI Products AquaGuard wound dressings received June–September 2021 were exposed to elevated storage temperatures that may have impacted product effectiveness. The FDA states adverse health consequences are unlikely.
Product
a. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR 7X7 (5/PK) 9CENCO Catalog #68751510104. b. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR BARR 10X12 (5/BX) Catalog #68751510105
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1796-2022·2022-10-05
Mckesson DermaCol Collagen Dressings Recalled for Storage Temperature Excursion
Mckesson recalls DermaCol collagen dressings exposed to temperature excursions during storage (June-August 2021). FDA stated adverse health consequences are unlikely.
Product
a. DERMARITE INDUSTRIES DermaCol Collagen Dressing DermaCol Without Border Collagen / Sodium Alginate / Carboxyl Methylcellulose (CMC) / Ethylenediamine-tetraacetic Acid (EDTA) 4 X 4 Inch 10 Count Model Number: 00303E. b. DERMARITE INDUSTRIES DermaCol Ag Silver Collagen…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V738000·2022-10-04
Contract Manufacturer Recalls 2023 Trailers With Incorrect Axle Size
Contract Manufacturer is recalling 2023 trailers because an incorrect axle size may have been installed, posing a crash risk if the axle breaks.
Product
CONTRACT MANUFACTURER — CONTRACT MANUFACTURER EQ14-17+3, TH10-20BK4CR, EQ16-17+3, TU10-20BK4CR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V736000·2022-10-04
Blue Bird Recalls 2013-2021 Vision School Buses for Fuel Leak Risk
Blue Bird is recalling 2013-2021 Vision school buses with Ford 6.8L LPG engines because a damaged fuel line may leak, increasing fire risk.
Product
BLUE BIRD — BLUE BIRD VISION, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V737000·2022-10-04
2022-2023 Coachmen Recreational Vehicles Recall: Unintended Awning Movement
Forest River is recalling certain 2022-2023 Coachmen recreational vehicles with a software issue that may cause the awning to unintentionally extend or retract while parked, increasing injury risk. Owners should contact dealers for a free ECM software update.
Product
COACHMEN — COACHMEN GALLERIA, NOVA, BEYOND
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V735000·2022-10-03
East Texas Recalls 2021 Tank Trailers Due to Axle Weld Defect
East Texas Trailer is recalling 2021 Tank trailers because a defective axle weld may crack or separate, increasing crash risk.
Product
EAST TEXAS — EAST TEXAS TANK TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E085000·2022-09-30
Meritor Recalls Front Non-Drive Steer Axles Due to Tie Rod Clamp Cracking
Meritor is recalling certain Front Non-Drive Steer Axles because improperly heat-treated tie rod clamps may crack and separate, potentially causing a sudden loss of steering.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide