State

Rhode Island product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40326–40350 of 76860

HighFDA (Devices)·Z-1463-2018·2018-05-02
Integra LifeSciences Recalls Humeral Stem Trials for Breakage Risk
Integra LifeSciences is recalling 1,619 humeral stem trials for the Titan Modular Shoulder System because they may break during surgery.
Product
The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog Number Product Description TRL092002506 Humeral Stem Trial, 6mm TRL092002507 Humeral Stem Trial, 7mm TRL092002508 Humeral Stem Trial, 8mm TRL092002509…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1503-2018·2018-05-02
Stryker T4 Pullover Toga Recall Due to Layer Separation
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Pullover Toga, Large; Catalog Number: 0400-760-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2018·2018-05-02
Zimmer Biomet Recalls Humeral Guide Wire Ball Tips Due to Packaging Seal Failure
Zimmer Biomet is recalling Humeral Guide Wire Ball Tips because the sterile packaging seal may fail, potentially compromising the device's sterility.
Product
Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length; Item Number: 47-2255-008-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1533-2018·2018-05-02
BD Vacutainer Blood Collection Set Recalled for Sterility Assurance Failure
Becton Dickinson is recalling BD Vacutainer Ultra Touch Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Product
BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12. Catalog no 367364
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E030000·2018-05-02
Ivolution Recalls IV2 HY-811 Motorcycle Helmets for Vision Blockage
Ivolution Sports Inc. is recalling IV2 HY-811 motorcycle helmets because they may block peripheral vision, increasing crash risk.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1133-2018·2018-05-02
Maharaja Food Importers Recalls Whole Wheat Parotta for Undeclared Milk
Maharaja Food Importers, Inc. is recalling Whole Wheat Parotta because the label lists ghee but fails to declare milk as an ingredient.
Product
WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1475-2018·2018-05-02
Zimmer Biomet Recalls Intramedullary Fixation Guide Wires Due to Packaging Seal Failure
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter, 100 cm Length; Item Number: 47-2237-033-00
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1497-2018·2018-05-02
Diagnostic Hybrids Recalls MicroVue CIC-C1q EIA Kits Due to Bacterial Contamination
Diagnostic Hybrids, Inc. is recalling 19 MicroVue CIC-C1q EIA kits because a component was found to contain bacterial contamination.
Product
MicroVue CIC-C1q EIA, Model A001. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. The MicroVue CIC-C1q EIA is for detection of circulating immune complexes (CIC) in human serum or plasma. In certain disease states…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0716-2018·2018-05-02
McKesson Recalls Diltiazem HCl Extended-Release Capsules Due to Dissolution Failures
McKesson Packaging Services is recalling Diltiazem HCl Extended-Release Capsules, 240 mg, because stability testing showed high dissolution results.
Product
Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0685-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints
Time-Cap Laboratories is recalling various strengths of ibuprofen tablets due to odor complaints related to CGMP deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0692-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints
Time-Cap Laboratories is recalling specific lots of Ibuprofen 800 mg tablets due to odor complaints linked to CGMP deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1467-2018·2018-05-02
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires due to potential sterile packaging seal failures.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length; Item Number: 47-2490-098-00
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1469-2018·2018-05-02
Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Packaging Seal Failure
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2490-097-00
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0695-2018·2018-05-02
Time-Cap Recalls Ibuprofen Caplets Due to Odor Complaints
Time-Cap Laboratories is recalling specific bottles of Ibuprofen 200 mg caplets due to odor complaints linked to CGMP deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1526-2018·2018-05-02
Stryker Recalls 18 Hinge Coupling Units Due to Packaging Error
Stryker GmbH is recalling 18 Hinge Coupling Hoffmann LRF units because connecting nuts were incorrectly packed in hinge coupling packaging.
Product
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1499-2018·2018-05-02
Diagnostic Hybrids Recalls MicroVue SC5b-9 Plus EIA Kits Due to Bacterial Contamination
Diagnostic Hybrids, Inc. is recalling 72 MicroVue SC5b-9 Plus EIA kits because a component was found to contain bacterial contamination.
Product
MicroVue SC5b-9 Plus EIA (CE-IVD), Model A029. An enzyme immunoassay for the quantitation of SC5b-9 complex present in human plasma or serum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0693-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints
Time-Cap Laboratories is recalling specific lots of 800 mg ibuprofen tablets due to odor complaints linked to CGMP deficiencies.
Product
Ibuprofen Tablets USP 800 mg, a) 100 tablet (NDC 42582-113-10) and b) 500 tablet (NDC 42582-113-18) bottles, Rx, Distributed by; Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0687-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints and CGMP Deficiencies
Time-Cap Laboratories is recalling specific lots of Ibuprofen Tablets USP 400 mg due to odor complaints related to Current Good Manufacturing Practice (CGMP) deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0690-2018·2018-05-02
Ibuprofen Tablets Recalled Due to Odor Complaints and CGMP Deficiencies
Time-Cap Laboratories is recalling specific lots of Ibuprofen Tablets USP 600 mg due to odor complaints linked to CGMP deficiencies.
Product
Ibuprofen Tablets USP 600 mg, a) 100 tablets (NDC 42582-112-10) and b) 500 tablet bottles (NDC 42582-112-18), Rx, Distributed by: Bi-Coastal Pharma International, Shrewsbury, NJ, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1519-2018·2018-05-02
Roche Acetaminophen Assay Method Sheets Missing Interference Statement
Roche Diagnostics is recalling Acetaminophen assay method sheets for COBAS INTEGRA and MODULAR ANALYTICS systems because they omit a statement regarding potential interference from gammopathy.
Product
Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas c Integra AAcetaminophen150 test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1521-2018·2018-05-02
Cook Inc. Recalls Advance 35LP Balloon Catheters Due to Labeling Error
Cook Inc. is recalling 40 Advance 35LP Low-Profile PTA Balloon Dilatation Catheters because some units were packaged with incorrect size labels.
Product
Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0; UDI: 10827002522647 and 10827002522524 Product Usage: The Advance¿ 35LP Low Profile PTA Balloon Dilation Catheter is indicated for percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1474-2018·2018-05-02
Zimmer Biomet Recalls Humeral Guide Wires Due to Sterile Packaging Seal Failure
Zimmer Biomet is recalling 19,483 M/DN Intramedullary Fixation Humeral Guide Wires because of a potential failure of the sterile packaging seal.
Product
M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter, 70 cm Length; Item Number: 00-2255-026-00
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0689-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints
Time-Cap Laboratories is recalling specific lots of Ibuprofen 600 mg tablets due to odor complaints linked to CGMP deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1511-2018·2018-05-02
Synthes Flex Arm Recalled for Potential Connection Failure
Synthes, Inc. is recalling 84 Flex Arm units because the quick connect feature may fail to connect to mating parts.
Product
Flex Arm Product Usage: The Synthes Flex Arm is a component of the Synthes Minimally Invasive Support System, which provides secure table mounting for minimally invasive spine surgery. The Flex Arm is designed to hold Synthes Minimally Invasive Retractors, which are…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0686-2018·2018-05-02
Time-Cap Recalls Ibuprofen Tablets Due to Odor Complaints
Time-Cap Laboratories is recalling specific lots of ibuprofen tablets due to odor complaints linked to CGMP deficiencies.
Product
IBUPROFEN — IBUPROFEN (IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide