State

Rhode Island product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40501–40525 of 76860

HighFDA (Devices)·Z-1344-2018·2018-04-18
ICU Medical Recalls 7-inch Intravascular Administration Sets with Incorrect Spin Collar
ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.
Product
7" Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item AH7262. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1367-2018·2018-04-18
Teleflex Medical Recalls Latex Rebreathing Bags Due to Missing Allergen Warning
Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.
Product
Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1356-2018·2018-04-18
Bard Feeding Tubes Recalled for Ineffective Connector Fusion
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Product
Bard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V245000·2018-04-18
Newmar Recalls Motorhomes Due to Headlight Beam Switching Defect
Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.
Product
NEWMAR — NEWMAR LONDON AIRE, DUTCH STAR, VENTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1349-2018·2018-04-18
Getinge Recalls VOLISTA StandOP Surgical Lights Due to Handle Detachment Risk
Getinge is recalling 5,214 VOLISTA StandOP surgical lights because the central handle holder can detach, potentially dropping particles into the sterile field during procedures.
Product
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901, ARD568811911 ARD568811951, ARD568811961 The device is designed to illuminate the body of a patient during surgical operations, diagnostics and treatment. These…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1355-2018·2018-04-18
Bard Infant Feeding Tube Recalled for Ineffective Connector Fusion
C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.
Product
Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1341-2018·2018-04-18
Beckman Coulter AQUIOS CL Flow Cytometer System Recalled for Sample ID Errors
Beckman Coulter is recalling 288 AQUIOS CL Flow Cytometer Systems because the single tube loader may process the same sample with two different IDs, potentially causing erroneous results.
Product
AQUIOS CL Flow Cytometer System, Catalog #B30166. The AQUIOS CL Flow Cytometer system is an automated analyzer that use a no-wash sample preparation process.The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18142·2018-04-18
Primark Recalls Decorative Cushions Due to Fire Hazard
Primark is recalling about 14,500 decorative cushions sold in the northeastern U.S. because they can catch fire if exposed to an ignition source.
Product
Decorative cushions
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2018·2018-04-18
Hill-Rom Progressa Bed Recall Due to Brake Component Failure Risk
Hill-Rom is recalling 2,117 Progressa adjustable hospital beds because a braking system component may break, causing unwanted bed movement and potential injury.
Product
Progressa Bed - AC-powered adjustable hospital bed
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V246000·2018-04-18
Riverside Recalls 2015-2017 Motorhomes Due to Fire Extinguisher Defects
Riverside RV is recalling 2015-2017 White Water, Water Fall, and Mt. McKinley motorhomes because certain fire extinguishers may clog or detach, posing injury risks.
Product
RIVERSIDE — RIVERSIDE WATER FALL, MT. MCKINLEY, WHITEWATER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1357-2018·2018-04-18
Bard Premature Infant Feeding Tubes Recalled for Ineffective Fusion
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Product
Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2018·2018-04-18
Beckman Coulter iQ200 Urine Analyzer Recall for Barcode Reading Failures
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers because they may fail to read dilution barcodes, causing erroneous results that could delay treatment.
Product
iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100, Catalog #s: 800-3046, 800-3047, 800-3052, 800-3053, 800-3802, 800-3803, 800-3900, 800-3920, 800-3925, 800-3931, 800-3933, 800-3934, 800-3935, 800-3937, 800-3950, 800-3951, 800-3042, 800-3043, 800-3044…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1354-2018·2018-04-18
Bard Premature Infant Feeding Tube Recalled for Ineffective Fusion
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Product
Bard(R) Premature Infant Feeding Tube, ENFit(TM), REF EN0036400 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0622-2018·2018-04-18
Elroselabs Recalls Molleave OTC Product Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Molleave, 2 oz bottles, due to current Good Manufacturing Practice (cGMP) deviations. The product was distributed nationwide.
Product
Molleave, 2 oz bottle, OTC, Manufactured for Elrose Labs, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1347-2018·2018-04-18
ICU Medical Recalls Infusion Sets with Incorrect Spin Collars
ICU Medical is recalling 7,600 sterile intravascular administration sets because they were manufactured with an incorrect spin collar. The sets were distributed in the US, Canada, and Japan.
Product
14 cm (5.5") Appx 0.27 ml, Smallbore Ext Set w/SURPLUG¿ Nano T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item IR-NG31481B, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0623-2018·2018-04-18
Elroselabs Recalls Conzerol Hydrogen Peroxide Gel Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Conzerol Hydrogen Peroxide Gel 3% nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3%, 1.5 oz. tube, OTC, Manufactured for Elrose Labs, Inc., Sanford, FL
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0621-2018·2018-04-18
Elroselabs Recalls Conzerol Topical Cream Due to Manufacturing Deviations
Elroselabs Inc. is voluntarily recalling Conzerol topical cream nationwide due to cGMP deviations. The recall was initiated in March 2018 and terminated in December 2020.
Product
Conzerol zero molluscum contagiosum, Topical Cream, Net weight 0.78 (22g), Elrose Labs, Sanford Fl 32771 USA --- NDC 70223-001-06
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1343-2018·2018-04-18
ICU Medical Recalls Infusion Sets with Incorrect Spin Collars
ICU Medical is recalling specific lots of sterile intravascular administration sets because they were manufactured with an incorrect spin collar.
Product
6.5" (17 cm) Appx. 0.57 ml, Trifuse Ext Set w/3 MicroClave¿ Clear, NanoClave¿ T-Connector, 4 Clamps, Rotating Luer, Item A1254, 50 pouches per case, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1353-2018·2018-04-18
Certified Safety Mfg Recalls First Aid Kits with Leaking Honeywell Eyewash
Certified Safety Mfg Inc is recalling 748 first aid and emergency kits containing Honeywell eyewash due to leaking bottles. The affected units were distributed nationwide.
Product
First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size: Honeywell Part# K206125 LXXV - 75V " Economy Cabinet 3 Shelf R508016 Eye Wash " 4 oz. 32-000452-0000 K 206154 LXXV - 75V " Deluxe Cabinet ¿3 Shelf RS08016 Eye…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1370-2018·2018-04-18
Teleflex Baker Jejunostomy Tubes Recalled for Missing Latex Warning
Teleflex Medical Europe Ltd is recalling 200 Baker Jejunostomy Tubes because the packaging lacks a required warning that the product contains natural rubber latex.
Product
Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1339-2018·2018-04-18
Ethicon Recalls PDS Plus Sutures Due to Incorrect Expiry Date Labeling
Ethicon, Inc. is recalling PDS Plus Antibacterial Sutures because three lots were labeled with a five-year expiry date instead of the correct two-year date.
Product
PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet 27 Single Armed OS-4 Needle
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1342-2018·2018-04-18
ICU Medical Recalls Smallbore Extension Sets with Incorrect Spin Collars
ICU Medical is recalling 11,500 smallbore extension sets manufactured with incorrect spin collars. The affected units were distributed in the US, Canada, and Japan.
Product
6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk Non-Sterile, 500 per case, Item A1009-NS, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1369-2018·2018-04-18
Teleflex Recalls Simplastic Suprapubic Puncture Instruments for Missing Latex Warning
Teleflex Medical Europe Ltd is recalling Simplastic Suprapubic Puncture Instruments because the packaging lacks a required warning that the products contain natural rubber latex.
Product
Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c) 650704160 551316 Product Usage: RUSCH Simplastic Suprapubic Puncture Instruments are indicated for emergency suprapubic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0624-2018·2018-04-18
FDA Recalls Zhong Hua Jiu Menthol Patches for GMP Deviations
United Pacific Co Ltd is recalling Zhong Hua Jiu (menthol 1%) Patches because they were produced with substandard GMP manufacturing processes.
Product
Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1345-2018·2018-04-18
ICU Medical Recalls 7-inch Smallbore Infusion Sets with Incorrect Spin Collar
ICU Medical is recalling 2,950 sterile 7-inch smallbore infusion sets because they were manufactured with an incorrect spin collar. The affected lots were distributed in the US, Canada, and Japan.
Product
7" Smallbore Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item B9900-629, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device…
Category
Medical Device
Distribution
Distributed nationwide