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.

53176–53200 of 76881

HighFDA (Food)·F-0202-2016·2015-11-25
National Frozen Foods Recalls Italian Blend for Listeria Risk
National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.
Product
Italian Blend. Product is IQF frozen, not ready to eat, each label carries cooking instruction. Label reads in part: "*** market pantry *** STEAM-IN-BAG Italian-Style Blend Broccoli, Cauliflower, Carrots, Italian-Style Green Beans & Zucchini*** NET WT 12 OZ***(UPC) 0 85239…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0207-2016·2015-11-25
National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Product
Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***MARKON FIRST CROP*** A proof of the label was provided, it does not contain product identity, net wt or ingredients. This product is available in…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·15V798000·2015-11-25
Forest River Recalls Motorhomes Due to Unstable Electric Entry Steps
Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.
Product
FOREST RIVER — FOREST RIVER, COACHMEN, SPORTSCOACH PATHFINDER, MIRADA, PRISM, PURSUIT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0206-2016·2015-11-25
National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk
National Frozen Foods Corporation is recalling Monarch and Valmont Italian Vegetable Blend due to potential Listeria monocytogenes contamination.
Product
Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part Item # 58108-03475 "***MONARCH***ITALIAN VEGETABLE BLEND CONTAINS ZUCCHINI, CARROTS, CAULIFLOWER, LIMA BEANS AND ITALIAN GREEN BEANS***NET WT***64…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0349-2016·2015-11-25
Downing Labs Recalls Taurine Injectable Due to Sterility Concerns
Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.
Product
Taurine Injectable, 50mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0290-2016·2015-11-25
Civco Medical Instruments Recalls Large Gauge Infiniti Plus Needle Guides
Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Product
CIVCO Sales Demo Kit. REF DEMOGPGUIDE Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ultrasound transducers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0208-2016·2015-11-25
National Frozen Foods Recalls Italian Vegetable Blend for Listeria Risk
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Product
Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***GARDEN FRESH***64775***47374***ITALIAN BLEND CONTAINS: ZUCCHINI, CARROTS, CAULIFLOWER, LIMAS, ITALIAN BEANS***20 LB NET WT***" No UPC on blue liner.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0286-2016·2015-11-25
Civco Infiniti Plus Needle Guide Recalled Due to Sterility Concerns
Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Product
CIVCO Infiniti Plus Needle Guide, Sterile Needle Guide, 12-18GA, Rx ONLY, STERILE EO. REFs 610-1215, 610-1234, 610-1235, 610-1236. Large Gauge Infiniti Plus Needle Guides, used in needle-guided (or catheter) procedures with diagnostic ultrasound transducers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0288-2016·2015-11-25
Civco Biopsy Starter Kit Recalled Due to Sterility Concerns
Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.
Product
CIVCO Biopsy Starter Kit, Reusable non-sterile bracket with Infiniti Plus (12, 14, 16, 18GA) needle guides, Rx ONLY. REFs 10787043, 11001906, 11001906(CMI), 613-247, 613-247(CMI), 620-116, 639-014, 639-016, 639-021, 639-024, 639-025, 639-026, 639-027, 639-033, 639-035, 639-047…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V797000·2015-11-25
Newmar Recalls 2016 King Aire Vehicles for Missing Emergency Exit Window
Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.
Product
NEWMAR — NEWMAR KING AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0262-2016·2015-11-25
US Compounding Recalls Lincomycin/Lidocaine Vials Due to Sterility Concerns
US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.
Product
Lincomycin/Lidocaine (300 mg/1%/mL), 10 mL Multi-Dose Vial, For IV Injection or IV Injection After Dilution, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3104-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0293-2016·2015-11-25
TZ Medical Neptune Plus Hemostasis Pad Recall for Labeling Mismatch
TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.
Product
Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0232-2016·2015-11-25
Qualitest Recalls Hydrochlorothiazide Capsules Due to Particulate Matter
Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.
Product
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0312-2016·2015-11-25
Ameditech Recalls Immutest Drug Screen Cups Due to Reduced Reactivity
Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.
Product
Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5; Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP; Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-12BUP; Immutest 5 panel, Item No. IMCA-5AB-W; Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0298-2016·2015-11-25
Ameditech Recalls 1 Step 12 Panel Cup Drug Tests
Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.
Product
1 Step 12 Panel Cup, Item No. NBCA-12M-W These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0311-2016·2015-11-25
Ameditech Recalls iCup Drug Screen Cups Due to Reduced Reactivity
Ameditech is recalling iCup drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Product
iCup Drug Screen Cup, Item No. I-DXA-187-016, I-DXA-167-013; iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142; iCup DX 11 Panel w/Adulterant, Item No. I-DXA-1117-131; iCup DX 12 Panel w/Adulterant, Item No. I-DXA-1127-023; iCup DX 6 Panel w/Adulterant, Item No.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0278-2016·2015-11-25
Ethicon Harmonic ACE+ 7 Laparoscopic Shears Recalled for Packaging Defect
Ethicon Endo-Surgery is recalling Harmonic ACE+ 7 Laparoscopic Shears because holes in the Tyvek packaging can compromise the sterile barrier.
Product
HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm, 36cm, 45cm length), Ethicon Endo-Surgery. Indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0234-2016·2015-11-25
Par Pharmaceutical Recalls Meclizine Hydrochloride Tablets Due to Impurity Failures
Par Pharmaceutical is recalling Meclizine Hydrochloride Tablets because they failed impurity specifications. The recall covers 100 and 1000-count bottles distributed nationwide.
Product
Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0300-2016·2015-11-25
Ameditech Recalls 11 Panel Drug Abuse Tests Due to Reduced Reactivity
Ameditech is recalling 11 Panel Drug Abuse Tests because they have shown reduced reactivity. The affected products are distributed in the US and Australia.
Product
11 Panel Cup (OPI2000) w/Adult, Item No. 71125AA2K ; and 11 Panel Cup (OPI300) w/Adult, Item No. 71125AA These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0318-2016·2015-11-25
TZ Medical Recalls SilverStat Hemostasis Pads Due to Labeling Discrepancy
TZ Medical Inc. is recalling 10,180 units of SilverStat hemostasis pads because the instructions for use did not match the original FDA submission.
Product
SilverStat, sterile 2" x 2 " calcium alginate hemostasis pad with sliver nitrate, Part number 8870-07. Product Usage: SilverStat is an effective barrier to microbial penetration for moderate to heavy exudating partial and full-thickness wounds, including pressure…
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-0303-2016·2015-11-25
Ameditech Recalls ArcPoint Labs 10 Panel Dip Screen Due to Reduced Reactivity
Ameditech is recalling ArcPoint Labs 10 Panel Dip Screen (OXY) drug tests because they have shown reduced reactivity.
Product
ArcPoint Labs 10 Panel Dip Screen (OXY), Item No. APD-10MO These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0315-2016·2015-11-25
Ameditech Recalls ProScreen Drug Panel Tests Due to Reduced Reactivity
Ameditech is recalling ProScreen drug panel tests because they have shown reduced reactivity. The recall covers 31,530 units distributed in the US and Australia.
Product
ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-10MMO-300, PSCup-10M, PSCupA-10MO, PSCUp-10AB; ProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM; ProScreen 10 Panel Dip Card, Item No. PSD-10MMO-300, PSD-10MOX…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0304-2016·2015-11-25
Ameditech Recalls CLIA RDTC 12-Panel Drug Abuse Tests for Reduced Reactivity
Ameditech is recalling 7,482 units of CLIA RDTC 12-Panel Cup drug abuse tests because they have shown reduced reactivity. The products were distributed in the US and Australia.
Product
CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12 These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0317-2016·2015-11-25
Ameditech Recalls Thermo Fisher 6 Drug Cassettes Due to Reduced Reactivity
Ameditech is recalling Thermo Fisher 6 Drug Cassettes because they have shown reduced reactivity. The recall affects 220 units distributed in the US and Australia.
Product
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU, MTPA-8MBAU These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0309-2016·2015-11-25
Ameditech Recalls DrugSmart Dip Drug Abuse Tests Due to Reduced Reactivity
Ameditech is recalling 160 units of DrugSmart Dip drug abuse tests because they have shown reduced reactivity. The affected products were distributed in the US and Australia.
Product
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D; DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of…
Category
Medical Device
Distribution
Distributed nationwide