State

Rhode Island product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34451–34475 of 76791

SevereFDA (Drugs)·D-1424-2019·2019-07-03
Premier Pharmacy Labs Recalls Phenylephrine Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 1,040 syringes of Phenylephrine HCL injection nationwide because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Phenylephrine HCL PF INJ in 0.9% Sodium Chloride, 1000mcg/10mL (100mgc/mL), *Contains Sulfites*, 10mL Single-Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-236-16, barcode 8 69623 23616 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1414-2019·2019-07-03
Premier Pharmacy Labs Recalls Dexamethasone Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 86 syringes of Dexamethasone Sodium Phosphate due to potential sterility issues found during an FDA inspection.
Product
Dexamethasone Sodium Phosphate Preservative Free Sterile Solution for INJ, 24mg/mL, 1mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-252-10, barcode 0 69623 25210 4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1421-2019·2019-07-03
Premier Pharmacy Labs Recalls Naloxone HCL Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling Naloxone HCL Preserved Injection because FDA inspections found insufficient environmental controls and lack of process validations, raising concerns about sterility assurance.
Product
Naloxone HCL Preserved INJ, 500mg/50mL (10mg/mL), 50mL Sterile MDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-235-39, barcode 6 69623 23539 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1412-2019·2019-07-03
Premier Pharmacy Labs Recalls Brilliant Blue Ophthalmic Injection for Sterility Concerns
Premier Pharmacy Labs is recalling 578 vials of Brilliant Blue Ophthalmic Injection due to a lack of assurance of sterility identified during an FDA inspection.
Product
Brilliant Blue Ophthalmic PF INJ, 0.5mg/mL (0.05%), 1 mL SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-211-31, barcode 2 69623 21131 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1425-2019·2019-07-03
Premier Pharmacy Labs Recalls Riboflavin 5-Phosphate Sodium Ophthalmic Solution
Premier Pharmacy Labs is recalling 125 bottles of Riboflavin 5-Phosphate Sodium Ophthalmic Solution due to a lack of assurance of sterility.
Product
Riboflavin 5-Phosphate Sodium Ophthalmic Solution, 19.05mg/3mL (6.35 mg/mL), 3 mL Dropper Bottle, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-106-61, barcode 1 69623 10661 9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1416-2019·2019-07-03
Premier Pharmacy Labs Recalls Isoproterenol Bags Due to Sterility Concerns
Premier Pharmacy Labs is recalling 606 bags of Isoproterenol HCL in D5W because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Isoproterenol HCL in D5W (Sterile to Sterile), 200mcg/50mL (4mcg/mL), 50mL Sterile Single-Dose Bag, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-230-57, barcode 0 69623 23057 7.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1434-2019·2019-07-03
American Health Packaging Recalls Pramipexole Dihydrochloride Tablets Due to GMP Deviations
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and possible cross-contamination from cleaning failures.
Product
Pramipexole Dihydrochloride Tablets, 1.0 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-982-95; NDC Carton: 68084-982-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1419-2019·2019-07-03
Premier Pharmacy Labs Recalls Lidocaine and Phenylephrine Injection Vials
Premier Pharmacy Labs is recalling 323 vials of Lidocaine 0.5%/Phenylephrine 0.75% Injection due to a lack of sterility assurance identified during an FDA inspection.
Product
Lidocaine 0.5%/Phenylephrine 0.75% P.F. INJ, 1mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-176-31, barcode 6 69623 17631 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1429-2019·2019-07-03
Acetaminophen Children's Liquid Recalled for Microbial Contamination Risk
H J Harkins Company is recalling 40 bottles of Acetaminophen Children's Liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Product
Acetaminophen Children's Liquid, 160 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057, NDC 52959-0309-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1428-2019·2019-07-03
Premier Pharmacy Labs Recalls Succinylcholine Chloride Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling 1,721 syringes of Succinylcholine Chloride due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
SUCCINYLcholine Chloride, 200mg/10mL (20mg/mL), 10mL Sterile Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-239-16, barcode 9 69623 23916 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1411-2019·2019-07-03
Premier Pharmacy Labs Recalls Atropine Sulfate Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 745 syringes of Atropine Sulfate Injection because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Atropine Sulfate PF INJ, 0.8 mg/2 mL (0.4 mg/mL), 2mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-131-12, barcode 0 69623 13112 6.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1210-2019·2019-07-03
Becton Dickinson Recalls SmartSite Syringe Administration Sets Due to Leaking
Becton Dickinson is recalling SmartSite Syringe Administration Sets because they may leak, potentially interrupting infusions or exposing healthcare workers to fluids.
Product
SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1433-2019·2019-07-03
Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and a cleaning procedure failure that may have caused cross-contamination.
Product
Pramipexole Dihydrochloride Tablets, 0.5 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-974-95; NDC Carton: 68084-974-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1430-2019·2019-07-03
Diphenhydramine Liquid Recalled for Potential Microbial Contamination
H J Harkins Company is recalling Diphenhydramine HCL Liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Product
Diphenhydramine HCL Liquid, 12.5 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057, NDC 52959-0123-03.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1422-2019·2019-07-03
Premier Pharmacy Labs Recalls Neostigmine Methylsulfate Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling Neostigmine Methylsulfate syringes nationwide due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
Neostigmine Methylsulfate, 5mg/5mL (1mg/mL), 5mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-234-15, barcode 5 69623 23415 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1423-2019·2019-07-03
Premier Pharmacy Labs Recalls Orphenadrine Citrate Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 4,363 syringes of Orphenadrine Citrate Sterile Injectable Solution because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*, 30mg/mL, 1mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-104-10, barcode 7 69623 10410 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1888-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V513000·2019-07-03
BMW Recalls Multiple Models for High Pressure Fuel Pump Defect
BMW is recalling specific 2019-2020 models because a high pressure fuel pump may not be properly attached, potentially causing a fuel leak and fire risk.
Product
BMW — BMW X5, M850I, X7, 750I
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1413-2019·2019-07-03
Premier Pharmacy Labs Recalls Chlorpromazine Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 824 vials of Chlorpromazine HCL Injection because an FDA inspection found insufficient environmental controls that may compromise sterility.
Product
ChlorproMAZINE HCL INJ, 25mg/mL, *Contains Sulfites*, 1mL in a 5mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-122-28, barcode 7 69623 12228 4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1415-2019·2019-07-03
Premier Pharmacy Labs Recalls Droperidol Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 2,315 syringes of Droperidol Injectable Sterile Solution because FDA inspections found insufficient environmental controls and lack of sterility assurance.
Product
Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.
Category
Drug
Distribution
Distributed nationwide
HighCPSC·19757·2019-07-03
The Company Store Recalls Girls' Pajama Sets for Flammability Violation
The Company Store is recalling about 2,500 girls' pajama sets because they fail to meet federal flammability standards, posing a burn risk.
Product
Girl's pajama sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2019·2019-07-03
GE Healthcare Recalls Replacement ECG Leadwires Due to Defibrillation Risk
GE Healthcare is recalling 58,045 replacement ECG leadwires worldwide because they may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.
Product
Replacement ECG leadwires with snap ends REF/Catalog Number Description 2106386-101 Replacement ECG Leadwire, snap, LL, AHA, 130 cm/ 51 in The reusable ECG leadwire sets enable ECG monitoring with GE equipment requiring rectangular 11-pin ECG trunk cable. Use leadwire sets…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1784-2019·2019-07-03
Collins Aerospace TASE 500 Imaging Systems Recalled for Laser Safety Error
Collins Aerospace is recalling TASE 500 Imaging systems because the Nominal Ocular Hazard Distance for the alignment laser was miscalculated.
Product
TASE 500 Imaging systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1852-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling two VOLISTA StandOP Surgical Lights because the light head coating may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model: VLT600SF AIM STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 12 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model: VST66SF AIM
Category
Medical Device
Distribution
Distributed nationwide