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Rubicon Research Private Limited

Rubicon Research Private Limited Recalls

All product recalls associated with Rubicon Research Private Limited.

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Recall Summary

Total Recalls

134

Past Year

Class I (Serious)

Most Recent

Sep 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 21–40 of 134 recalls

Metoprolol Tablets (Rubicon) – Metal Contamination (2024)

Presence of Foreign Substance: metal in tablet

Class IIModerate

FDAMay 6, 2024Nationwide• Rubicon Research Private Limited

Tramadol Tablets (Rubicon) – Foreign Tablet Presence (2024)

Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bottle of 1000-count tramadol

Class IIModerate

FDAApr 26, 2024Nationwide• Rubicon Research Private Limited

SURGIFOAM Gelatin Powder Kit (Ethicon) – Applicator Seal (2024)

Some applicator tips from these lots had open seals.

Low

123 4...7

Page 2 of 7Next

FDA

Apr 23, 2024

Nationwide

• Ethicon, Inc. Us

STRATAFIX Spiral MONOCRYL Plus (Ethicon) – Sterility Compromise (2024)

Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility

High

FDAMar 8, 2024CO, GA, IA +6 more• Ethicon, Inc.

ENDOPATH Echelon Reloads (Ethicon) – Staple Line Formation Risk (2023)

There is the potential for incomplete staple line formation during the firing sequence, without most or all staples, which may lead to insufficient tissue apposition that could require surgical intervention. This may result in bleeding, prolonged surgery, or surgical delay.

High

FDADec 11, 2023Nationwide• Ethicon Endo-Surgery Inc

PDS Plus Antibacterial Suture (Ethicon) – Tensile Strength Failure (2023)

Internal testing on returned product from this lot confirmed that some PDS" II (polydioxanone) Sutures from this lot did not meet tensile strength requirement.

FDAAug 10, 2023Nationwide• ETHICON, LLC

PDS II Suture (Ethicon) – Tensile Strength Failure (2023)

Internal testing on returned product from this lot confirmed that some PDS" II (polydioxanone) Sutures from this lot did not meet tensile strength requirement.

FDAAug 10, 2023Nationwide• ETHICON, LLC

PDS Plus Antibacterial Suture (Ethicon) – Breakage Risk (2023)

Suture breakage during intra-operative use could result in poor performance of the impacted product because the intended benefit of tissue approximation and/or ligation may not be achieved

FDAMar 31, 2023IN• Ethicon, Inc.

PDS II Suture (Ethicon) – Knot Tensile Weakness (2022)

knot tensile strengths were observed to be significantly below the minimum knot tensile, will result in breakage prior to use or intra-operatively rather than premature post-operative breakage

FDANov 16, 2022Nationwide• Ethicon, Inc. Us

STRATAFIX SPIRAL PGA-PCL (Ethicon) – Incorrect Needle Type (2022)

Laceration Risk

Packages may contain a PS-1 cutting edge needle and not the intended SH taper point needle may result in more tissue trauma than is anticipated for taper point needles, which may necessitate repair

FDASep 20, 2022Nationwide• Ethicon, Inc. Us

PDS II Suture (Ethicon) – Material Error (2022)

Product may contain the incorrect material which could impact treatment.

FDAAug 8, 2022IN• Ethicon, Inc. Us

CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD in... (Menarini Silicon Biosystems) – high number of total images/unassigne... (2022)

High number of total images/unassigned events including (dual positives) and the potential for false positive results being placed into the image gallery in some patient samples

FDAMay 20, 2022CA, FL, IL +9 more• Menarini Silicon Biosystems

STRATAFIX Spiral Suture (Ethicon) – component mix-up (2022)

Affected product lots may contain the incorrect needle type/size and suture length due to component mix-up.

FDAMar 24, 2022IN• Ethicon, Inc. Us

Metoprolol Tablets (Rubicon Research) – Metal Embedded (2021)

Complaint received of foreign matter (metal) embedded in tablet.

Class IIModerate

FDADec 31, 2021Nationwide• Rubicon Research Private Limited

RICON WHEELCHAIR LIFT Equipment Recall: EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR LIFT/RAMP

Ricon Corporation (Ricon) is recalling certain Baylift Wheelchair Lift, part number RISSBF3XXX-XX. The outer barrier cannot withstand the maximum force when fully deployed. As such, these lifts fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 403, "Platform Lift Systems."

NHTSAJul 23, 2021Nationwide• RICON

Ethicon Endo-Surgery Inc: HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated fo...

Fire/Burn Risk

An internal component may be cracked and become lodged behind the energy button potentially resulting in continuous activation of the device, may result in burns

FDAJul 20, 2021Nationwide• Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc: HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for...

Fire/Burn Risk

An internal component may be cracked and become lodged behind the energy button potentially resulting in continuous activation of the device, may result in burns

FDAJul 20, 2021Nationwide• Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc: ECHELON FLEX Powered Plus Stapler-intended for transectio...

Mislabeled: Labeled on the package as 60mm contains 45mm devices

FDAJun 3, 2021Nationwide• Ethicon Endo-Surgery Inc

Ethicon, Inc. Us: Ethicon Dermabond Advanced Topical Skin Adhesive-topical ...

Product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach

FDAJan 4, 2021Nationwide• Ethicon, Inc. Us

Ethicon, Inc. Us: PROCEED Surgical Mesh Hernia Mesh Oval, 15 cm x 20 cm

The firm is recalling the PROCEED Surgical Mesh device, because it is a sterile device, and a customer found a hair inside of the primary packaging of a single unit.

FDAOct 23, 2020IN• Ethicon, Inc. Us