State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48051–48075 of 76871

SevereFDA (Drugs)·D-0042-2017·2016-10-19
Pharmedium Recalls Fentanyl Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 1,735 syringes of fentanyl citrate because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
fentaNYL Citrate, 5 mcg per mL, 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3479.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0090-2017·2016-10-19
Pharmedium Recalls Succinylcholine Chloride Injection Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 2,495 syringes of succinylcholine chloride injection because stability data does not support the expiration dates, posing a risk of loss of potency.
Product
succinylcholine Chloride Injection, 20 mg per mL, 100 mg per 5 mL, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3357.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0024-2017·2016-10-19
Teva Recalls Amikacin Sulfate Injection Due to Manufacturing Deviations
Teva Pharmaceuticals USA is voluntarily recalling 11,844 vials of Amikacin Sulfate Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Amikacin Sulfate Injection, USP, 1 gm/4 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-9040-01 (individual pack), NDC 0703-9040-03 (shelf-pack carton of 10 vials).
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0070-2017·2016-10-19
Pharmedium Recalls Methadone Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 7,006 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
methadone HCl, 1 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6120.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0036-2017·2016-10-19
Pharmedium Recalls Fentanyl Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 110 syringes of fentanyl citrate because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
fentaNYL Citrate, 25 mcg per mL in 0.9% Sodium chloride, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3236.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0056-2017·2016-10-19
Pharmedium Recalls Ketamine HCl Injection Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 12,173 syringes of ketamine HCl Injection because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
ketamine HCl Injection, 50 mg per mL, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3348.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0100-2017·2016-10-19
Allergan Recalls Tazorac Gel 0.05% Due to Content Uniformity Failures
Allergan Sales, LLC is recalling 17,112 tubes of Tazorac (tazarotene) Gel 0.05% because the product failed content uniformity specifications.
Product
TAZORAC (tazarotene) Gel 0.05%, Rx only, packaged in 15 x 3.5 g professional sample containers, Manufactured by: Allergan Inc., Irvine, CA 92512. UPC: 300238335159.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0010-2017·2016-10-19
Leiter's Compounding Recalls Atropine Sulfate Ophthalmic Solution Due to Sterility Concerns
Leiter's Compounding is recalling Atropine Sulfate 0.01% ophthalmic solution because the filters used to produce the products were recalled, raising concerns about sterility.
Product
Atropine Sulfate 0.01% in 0.9% Sodium Chloride (Ophthalmic Solution) 10 mL Total Volume in a 15 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-011-39
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0023-2017·2016-10-19
Teva Recalls Amikacin Sulfate Injection Due to Manufacturing Deviations
Teva Pharmaceuticals USA is voluntarily recalling 27,547 vials of Amikacin Sulfate Injection due to CGMP deviations. The recall covers lots distributed nationwide and in Puerto Rico.
Product
Amikacin Sulfate Injection, USP, 500 mg/2 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-9032-01 (individual pack), NDC 0703-9032-03 (shelf-pack carton of 10 vials).
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V758000·2016-10-19
Mercedes-Benz Recalls 2017 E300 Sedans for Fuel Pump Wiring Defect
Mercedes-Benz is recalling 2017 E300 Sedans because the rear seat frame may damage fuel pump wiring, potentially causing an engine stall and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0091-2017·2016-10-19
Pharmedium Recalls Lidocaine Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 4,400 syringes of lidocaine HCl 1% because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
lidocaine HCl, 1%, in 0.9% Sodium Chloride, Preservative Free, Total Volume 3 mL in a syringe, Rx only, PharMEDium, Product code 2R3343.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0073-2017·2016-10-19
Pharmedium Recalls Midazolam Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 1,700 syringes of midazolam HCl because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
midazolam HCl, 1 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3196.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0080-2017·2016-10-19
Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 545 syringes of morphine sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
morphine Sulfate, 1 mg per mL (2 mg per 2 mL), in 0.9% Sodium Chloride, Preservative Free, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3353.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0093-2017·2016-10-19
Pharmedium Recalls Subpotent Fentanyl Citrate Syringes Nationwide
Pharmedium Services, LLC is recalling 500 syringes of fentanyl citrate due to confirmed subpotency. The product was distributed nationwide.
Product
fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3174.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0015-2017·2016-10-19
Leiter's Compounding Recalls Mitomycin Injection Due to Sterility Concerns
Leiter's Compounding is recalling Mitomycin 0.02% injections because the filters used to produce them were recalled, raising concerns about sterility.
Product
Mitomycin 0.02% (0.2 mg/mL) in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-005-35
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0078-2017·2016-10-19
Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 592 syringes of morphine sulfate because stability data does not support the expiry date, posing a risk of loss of potency.
Product
morphine Sulfate, 1 mg per mL (5 mg per 5 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 5 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3181.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0069-2017·2016-10-19
Pharmedium Recalls Lidocaine HCl Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 3,159 syringes of lidocaine HCl 2% because stability data does not support the expiry date, posing a risk of reduced potency.
Product
lidocaine HCl, 2%, 20 mg per mL (60 mg per 3 mL), 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2R3450.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0039-2017·2016-10-19
Pharmedium Recalls Fentanyl Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 1,522 syringes of fentanyl citrate because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
fentaNYL Citrate, 5 mcg per mL, 15 mcg per 3mL, in 0.9% Sodium chloride, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3318.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0012-2017·2016-10-19
Leiter's Compounding Recalls Cefuroxime Sodium Injection Due to Sterility Concerns
Leiter's Compounding is recalling Cefuroxime Sodium Injection because products were made with recalled filters, raising sterility concerns.
Product
Cefuroxime Sodium 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-007-35
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0017-2017·2016-10-19
Leiter's Compounds Recalls Prednisolone Placebo Due to Sterility Concerns
Leiter's Compounding is recalling placebo ophthalmic suspensions because they were produced using recalled filters, raising concerns about sterility.
Product
Placebo for Prednisolone Acetate 1%, Oph Suspension, 10 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0025-2017·2016-10-19
Pharmedium Recalls Atropine Sulfate Injection Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 4,407 syringes of atropine sulfate injection nationwide because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
atropine Sulfate Injection, 0.4 mg per mL, 1 mg per 2.5 mL, 2.5 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3324.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0085-2017·2016-10-19
Pharmedium Recalls Phenylephrine Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 380 syringes of Phenylephrine HCl because stability data does not support the expiry date, posing a potential loss of potency.
Product
PHENYLephrine HCl, 40 mcg per mL, 200 mcg per 5 mL, in 0.9% Sodium Chloride, Preservative Free, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3376.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0080-2017·2016-10-19
Contour Zero-Gravity Radiation Protection System Recalled for Cable Failure Risk
Contour Fabricators is recalling 447 Zero-Gravity radiation protection systems because excessive cable rotation may cause the shield to fall, posing an injury risk.
Product
Zero-Gravity Radiation Protection System Radiology Personnel protective shield.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0054-2017·2016-10-19
Publix Almond Strip Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Publix Almond Strip Danish due to the presence of small metal shavings.
Product
Publix Almond Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0071-2017·2016-10-19
GE OEC Brivo Mobile C-Arm X-Ray Recall for Uncontrolled Motion
GE Healthcare is recalling 148 OEC Brivo mobile C-arm X-ray units because a circuit board failure may cause the C-arm to move vertically without command.
Product
OEC Brivo 715 Prime, OEC Brivo 785 Essential, OEC Brivo 865 Advance Product Usage: The OEC Brivo Mobile C-Arm X-Ray Products are designed to provide digital spot film imaging and fluoroscopic image guidance for all adult and pediatric populations for orientations between…
Category
Medical Device
Distribution
Distributed nationwide