State

Rhode Island product recalls

73,598 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,048
Critical: 221
Severe: 707
Most recent: 2026-10-21

Of the 3,048 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 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27851–27875 of 76646

HighFDA (Devices)·Z-0423-2021·2020-11-11
3M Red Dot Monitoring Electrode Recall Due to Corrosion Risk
3M is recalling Red Dot Monitoring Electrodes because corrosion could cause performance failures in the ECG monitoring product.
Product
3M Red Dot Monitoring Electrode with Foam Tape - Product Usage: intended to be used by healthcare professionals for ECG monitoring. 50 electrodes per pouch; 20 pouches per shipper box (1000 electrodes total).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0361-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Cup Hip Prosthesis Components
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D. Cup with Spacers, 47 mm Number: 00-8065-644-26
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0357-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling specific acetabular cup hip prosthesis components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D. Cup with Spacers, 43 mm Number: 00-8065-640-22
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0349-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D. Cup with Spacers, 59 mm Number: 00-8065-556-22
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0354-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 61 mm Number: 00-8065-558-26
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Cup Hip Prosthesis Components
Zimmer Biomet is recalling 412 acetabular cup hip prosthesis components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 degree inclined face, O.D. Cup with Spacers, 57 mm Number: 00-8065-654-26
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0324-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Component Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling specific ZCA All Poly Acetabular Cup hip prosthesis components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D. Cup with Spacers, 45mm Item Number: 00-8065-542-22 Hip prosthesis component
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0391-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Snap-In O.D. Cup with Spacers, 49 mm Number: 00-8065-946-32
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns
Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 53 mm Number: 00-8065-650-32
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0327-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns
Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 47 mm Item Number: 00-8065-544-26
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0350-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 acetabular hip cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 59 mm Number: 00-8065-556-26
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0362-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Cups Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D. Cup with Spacers, 47 mm Number: 00-8065-644-28
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0386-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 59 mm Number: 00-8065-656-32
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0363-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cup Components Due to Sterilant Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D. Cup with Spacers, 49 mm Number: 00-8065-646-22
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0337-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D. Cup with Spacers, 53 mm Item Number: 00-8065-550-22
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0395-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Snap-In O.D. Cup with Spacers, 57 mm Number: 00-8065-954-32
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0418-2021·2020-11-11
Angiodynamics 5F Micro-Introducer Kits Recalled for Incorrect Device Packaging
Angiodynamics, Inc. is recalling 32 kits of 5F Standard Micro-Introducer Kits because they may contain a 4F Sheath/Dilator component instead of the correct device.
Product
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0321-2021·2020-11-11
Primus Ultra2 Resolution Variants System Recalled for Lack of FDA Clearance
Primus Corporation is recalling 97 Ultra2 Resolution Variants Systems because the devices did not receive FDA pre-market approval or clearance.
Product
Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation
Category
Medical Device
Distribution
20 states
ModerateFDA (Drugs)·D-0075-2021·2020-11-11
Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specification
Zydus Pharmaceuticals is recalling 7,908 cartons of Lansoprazole 30 mg tablets because they failed to meet dissolution specifications.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0074-2021·2020-11-11
Zydus Recalls Lansoprazole Tablets Due to Failed Dissolution Specification
Zydus Pharmaceuticals is recalling 6,840 cartons of Lansoprazole 15 mg tablets because they failed to meet dissolution specifications.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0402-2021·2020-11-11
Microbiologics Recalls Klebsiella Pneumoniae Strain Due to Incorrect VIM-1 Status
Microbiologics Inc is recalling 46 units of a Klebsiella pneumoniae strain because it is VIM-1 negative instead of the expected VIM-1 positive status.
Product
Catalog 02145P, Klebsiella pneumoniae derived from NCTC 13439 - Product Usage: intended to be used as controls to verify the performance of assays, reagents or media that are intended to be used in microbial testing for the detection and identification of a cultured…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0064-2021·2020-11-11
Teligent Pharma Recalls Fluocinonide Ointment Due to Impurity
Teligent Pharma is recalling Fluocinonide Ointment USP 0.05% due to out-of-specification impurity results.
Product
Fluocinonide Ointment USP 0.05%, packaged in: a) 15 gm tube, NDC 52565-0040-15, b) 30 gm tube, NDC 52565-0040-30 c) 60 gram tube, NDC 52565-0040-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0066-2021·2020-11-11
Jubilant Recalls Subpotent Olanzapine Orally Disintegrating Tablets Nationwide
Jubilant Cadista Pharmaceuticals is voluntarily recalling 23,616 blister packs of Olanzapine Orally Disintegrating Tablets, 5 mg, because the product was found to be subpotent.
Product
Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee, India, Marketed by: Jubilant Cardista Pharmaceuticals, Inc., Salisbury, MD NDC 59746-0306-32
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·21024·2020-11-10
Kohl's Recalls SONOMA Goods For Life Three-Wick Candles Due to Fire Hazards
Kohl's is recalling approximately 512,000 SONOMA Goods For Life three-wick candles because high flames can ignite wax or break glass, posing fire and burn risks.
Product
SONOMA Goods For Life branded three-wick candles
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·21028·2020-11-10
Ring Recalls 2nd Generation Video Doorbells Due to Fire Hazard
Ring is recalling approximately 350,000 2nd Generation Video Doorbells because incorrect installation screws can cause the battery to overheat, posing fire and burn risks.
Product
Ring Video Doorbells (2nd Generation)
Category
Consumer Product
Distribution
Distributed nationwide