State

Rhode Island product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52476–52500 of 76881

ModerateFDA (Devices)·Z-0603-2016·2016-01-13
Steris Amsco Warming Cabinet Recalled for Incorrect Temperature Labeling
Steris Corporation is recalling Amsco Warming Cabinets because the quick reference magnet displays incorrect Fahrenheit to Celsius conversions and default temperatures.
Product
AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the temperature of blankets, linens and sterile surgical IV/irrigation solutions to an acceptable level for various surgical, obstetrical, emergency, critical care and other healthcare applications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0602-2016·2016-01-13
Ethicon Recalls Gynecare Thermachoice III Uterine Balloon Therapy System
Ethicon, Inc. is recalling the Gynecare Thermachoice III Uterine Balloon Therapy System because stability data does not support the labeled two-year shelf life.
Product
Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon, Inc. The GYNECARE THERMACHOICE¿ III Uterine Balloon Therapy (UBT) System is a thermal balloon ablation device intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0613-2016·2016-01-13
Siemens Acute Care CKMB TestPak Recalled for Barcode Scanning Issues
Siemens Healthcare Diagnostics is recalling 1,051 units of Acute Care CKMB TestPaks because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care CKMB TestPak- in vitro diagnostic test for the measurement of the MB isoenzyme of creatine kinase (ATP: Creatine NPhosphostransferase, E. C. No. 2.7 .3.2) in heparinized plasma Catalog Number: CCKMB SMN:10445068
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0612-2016·2016-01-13
Siemens Acute Care MYO TestPak Barcode Labels May Not Scan
Siemens Healthcare Diagnostics Inc is recalling 608 units of Acute Care MYO TestPaks because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma Catalog Number: CMYO SMN:10445079
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0561-2016·2016-01-13
PD-Rx Pharmaceuticals Recalls Azithromycin 500 mg Tablets for cGMP Deviations
PD-Rx Pharmaceuticals is recalling Azithromycin 500 mg tablets because the original manufacturer did not adequately investigate customer complaints, resulting in cGMP deviations.
Product
Azithromycin 500 mg tablets, Rx Only, packaged in a) 1 count, b) 2 count, c) 3 count, and d) 7 count bottles, Packaged by: PD-RX Pharmaceuticals, Inc., Oklahoma City, OK 73127, Mfr: Wokhardt Ltd., Mumbai, India, NDC: a) 55289-274-79, b) 55289-274-02, c) 55289-274-03, d)…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0611-2016·2016-01-13
Siemens Acute Care DDMR TestPak Barcode Scanning Recall
Siemens Healthcare Diagnostics is recalling Acute Care DDMR TestPaks because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0608-2016·2016-01-13
Otto Bock Recalls Modular Polycentric EBS Knee Joints Due to Service Error
Otto Bock is recalling 40 Modular Polycentric EBS Knee Joints serviced between April 2015 and November 2015 because the wrong Loctite was used during repair.
Product
Ottobock Modular Polycentric EBS Knee Joint 3R60, 3R60=ST, 3R60=KD, 3R60=HD. Used for the prosthetic fitting of amputations of the lower. limb.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0616-2016·2016-01-13
Siemens Acute Care CCRP CalPak Recall for Barcode Scanning Issues
Siemens is recalling 65 units of Acute Care CCRP CalPak because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus CS analyzer Catalog Number: CCCRP-C SMN:10445067
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0606-2016·2016-01-13
Baxter INTERLINK Y-Type Solution Set Recalled for Particulate Matter
Baxter Healthcare is recalling INTERLINK Y-Type Solution Sets due to potential dark particulate matter on the spike adapter.
Product
Baxter INTERLINK System, Y-Type Solution Set, 78 (2.0 m), 2 Injection Sites, Male Luer Lock Adapter, 1C8581 s, Product Usage: C8581: For the administration of fluids from a container into the patients vascular system through a vascular access device. .
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2016·2016-01-13
Siemens Acute Care BHCG TestPak Recalled for Barcode Scanning Issues
Siemens Healthcare Diagnostics is recalling 590 units of Acute Care BHCG TestPak because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended to be used for calibration of the Stratus¿ CS Acute Care hCG method Catalog Number: CBHCG SMN:10445060
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0617-2016·2016-01-13
Siemens Acute Care BHCG CalPak Recalled Due to Barcode Scanning Issues
Siemens Healthcare Diagnostics Inc. is recalling 196 units of the Acute Care BHCG CalPak because the cartridge barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to be used for calibration of the Stratus¿ CS Acute Care rM ~ h CG method Catalog Number: CBHCG-C SMN:10445061
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0560-2016·2016-01-13
PD-Rx Recalls Azithromycin Tablets Due to Inadequate Complaint Investigation
PD-Rx Pharmaceuticals is recalling 45,022 bottles of Azithromycin Tablets, USP, 250 mg, because the manufacturer did not adequately investigate customer complaints.
Product
Azithromycin Tablets, USP, 250 mg, Rx Only, packaged in a) 2 count and b) 4 count bottles, Packaged by: PD-RX Pharmaceuticals, Inc., Oklahoma City, OK, 73127, Mfg: Wockhardt Ltd., Mumbai, India, NDC: a) 55289-964-02, b) 55289-964-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0609-2016·2016-01-13
Siemens Acute Care CTNI TestPak Barcode Scanning Recall
Siemens Healthcare Diagnostics Inc is recalling 5,558 units of the Acute Care CTNI TestPak because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma Catalog Number: CCTNI SMN: 10445071
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0607-2016·2016-01-13
Baxter CLEARLINK Blood Bag Spike Adapter Recalled for Particulate Matter
Baxter Healthcare is recalling CLEARLINK Blood Bag Spike Adapters due to potential dark loose particulate matter on the spike.
Product
Baxter CLEARLINK System, Blood Bag Spike Adapter, Luer Activated Valve for I.C. Access, 1C8687, Product Usage: C8687: An accessory to transfer a medicinal product from one container to another container.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0591-2016·2016-01-13
Biomet 3i Protection Caps Recalled for Inadequate Biocompatibility Testing
Biomet 3i is recalling specific Protection Caps due to inadequate biocompatibility testing. The devices are distributed worldwide, including the US.
Product
BIOMET 3i, PROVIDE PROTECTION CAP, Catalog # PPC484, PPC485, PPC654, and PPC655 BIOMET 3i Restorative Products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible. Provisional Abutments are intended for use as an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0618-2016·2016-01-13
Siemens Acute Care MYO DilPak Recall Due to Barcode Scanning Issues
Siemens Healthcare Diagnostics Inc is recalling 192 units of Acute Care MYO DilPak in vitro diagnostic products because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0619-2016·2016-01-13
Siemens Acute Care CKMB DilPak Recalled for Barcode Scanning Issues
Siemens Healthcare Diagnostics Inc. is recalling 146 units of the Acute Care CKMB DilPak because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care CKMB DilPak- an in vitro diagnostic product intended to be used in conjunction with the Acute Care CKMB TestPak Catalog Number: CCKMB-D SMN: 10445070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0582-2016·2016-01-13
Vidco MDP 2000 Remote Patient Monitoring Systems Recalled for Freezing
Vidco, Inc. is recalling 59 MDP 2000 Series Remote Patient Monitoring Systems because they may freeze and fail to reset without a power cycle.
Product
Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, or PGM340R4. The MDP2000 is intended for use in conjunction with patient monitoring equipment. The MDP2000 is not patient connected Examples of areas where the MDP200 is used include ICU…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0585-2016·2016-01-13
Synthes 13.5mm Medullary Reamer Head Recalled for Dimensional Mismatch
Synthes (USA) Products LLC is recalling 65 units of 13.5mm Medullary Reamer Heads that are actually 14mm. The devices are distributed nationwide.
Product
SYNTHES; 13.5MM Medullary Reamer Head; 352.135 NON STERILE. Part of the Flexible Reamer Set for orthopedic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0584-2016·2016-01-13
Smith & Nephew Recalls Mislabelled Birmingham Hip Resurfacing Modular Heads
Smith & Nephew is recalling 16 Birmingham Hip Resurfacing Modular Heads in the US because they were incorrectly labeled as a different device type not cleared for US marketing.
Product
BIRMINGHAM HIP RESURFACING MODULAR HEAD, REF numbers: 74121238, MODULAR HEAD 38 MM -8MM 74121242, MODULAR HEAD 42 MM -8MM 74121246, MODULAR HEAD 46 MM -8MM 74121250, MODULAR HEAD 50 MM -8MM 74121254, MODULAR HEAD 54 MM -8MM 74121258, MODULAR HEAD 58 MM -8MM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0610-2016·2016-01-13
Siemens Acute Care pBNP TestPak Recalled Due to Barcode Scanning Issues
Siemens Healthcare Diagnostics Inc is recalling 1,157 Acute Care pBNP TestPaks because their barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care pBNP TestPak- in vitro diagnostic test for the quantitative measurement of N-terminal pro-brain natriuretic peptide (NTproBNP) in heparinized plasma. Catalog Number: CPBNPM SMN: 10445086
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0614-2016·2016-01-13
Siemens Acute Care CCRP TestPak Recalled for Barcode Scanning Issues
Siemens Healthcare Diagnostics Inc is recalling 78 units of the Acute Care CCRP TestPak because barcode labels may not scan on Stratus CS systems.
Product
Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus¿ CS analyzer Catalog Number: CCCRP SMN:10445066
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0562-2016·2016-01-13
Freedom Pharmaceuticals Recalls Subpotent 5-methyltetrahydrofolate Calcium Drug
Freedom Pharmaceuticals is voluntarily recalling specific lots of 5-methyltetrahydrofolate Calcium because the drug was found to be subpotent.
Product
5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container NDC: 52372-0855-04; (b) 5 gm in 2 oz container NDC: 52372-0855-02; (c) 25 gm in 4 oz container NDC: 52372-0855-02, Rx only; Manufactured by: Hangzhou Dayangchem Co., Ltd. 328 Wener Rd, Xihu, Hangzhou, Zhejiang…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0583-2016·2016-01-13
Ultradent Recalls InterGuard Dental Refills Due to Manufacturing Defect
Ultradent is recalling InterGuard 5.5mm Econo Refills because the floss tether hole was not completely punched through.
Product
InterGuard 5.5mm Econo Refill, sizes, 4.0mm for short anatomical crowns and 5.5mm, part # 4012 Product Usage: InterGuard is a preventive aid for operative dentistry. It is used to protect adjacent teeth from iatrogenic preparation damage. This includes cavity and tunnel…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16E001000·2016-01-12
Wells Recalls Brake Light Switches for Potential Failure to Illuminate
Wells Vehicle Electronics is recalling specific brake light switches that may fail to illuminate brake lights or disengage cruise control, increasing crash risk.
Product
EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
Category
Vehicle
Distribution
Distributed nationwide