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Kingtec Group Vietnam Co. LTD, of Ben Cat Town, of Binh Duong Province, Vietnam

Kingtec Group Vietnam Co. LTD, of Ben Cat Town, of Binh Duong Province, Vietnam Recalls

All product recalls associated with Kingtec Group Vietnam Co. LTD, of Ben Cat Town, of Binh Duong Province, Vietnam.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

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 2781–2800 of 7756 recalls

6-Foot Seminar Tables (Lifetime) – injury risk (2021)

This recall involves Lifetime Products 6-Foot Seminar Tables with model #80176. The tables have gray metal frames and white plastic tops. The tables measure 6 feet long by 18 inches wide by 28 inches high. The "Lifetime" logo is molded into each end of the upper surface of the table top. A green product ID sticker located on the underside of the table has the model number and the year and chronological day of manufacture in the first five digits (Example: June 23, 2020 = 20175), followed by a two-digit number for the factory. The recalled tables were manufactured between August 7, 2016 (16220) and June 23, 2020 (20175).

CPSCMar 10, 2021Nationwide• Kingtec Group Vietnam Co. LTD, of Ben Cat Town, of Binh Duong Province, Vietnam

Boston Scientific Corporation: MAMBA Microcatheter. Packaged with protective sleeve ove...

The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.

FDAMar 5, 2021Nationwide• Boston Scientific Corporation

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Boston Scientific Corporation: MAMBA Flex 135 Microcatheter. Packaged with protective s...

The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.

FDAMar 5, 2021Nationwide• Boston Scientific Corporation

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use On...

Patient related messages created in RayCare 3B, RayCare 4A will be lost when upgrading from RayCare 2 to RayCare 3B or later

FDAMar 3, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

James Leckey Design Ltd 19C Ballinderry Road Lisburn United Kingdom: MyWay Walker Chassis - Product Usage: is intended for use...

Due to a failure of the welds, the casters detached from the rear legs of the walker.

FDAMar 1, 2021Nationwide• James Leckey Design Ltd 19C Ballinderry Road Lisburn United Kingdom

Brainlab AG Olof-palme-str. 9 Munich Germany: ExacTrac Dynamic (Medical Charged-Particle Radiation Ther...

In case of a failed automatic marker detection, a software error causes parts of the display to incorrectly behave as if the current patient position is within predefined tolerances and may allow the user to proceed to treatment despite potentially exceeding shift values.

FDAMar 1, 2021AZ, AR, CA +5 more• Brainlab AG Olof-palme-str. 9 Munich Germany

Sweet Heat Pepper Dip (B&G) – Undeclared milk (2021)

Cream Cheese and Sour Cream are declared, but milk is not declared on label.

Class IIModerate

FDAFeb 27, 2021ID, IN, WA• B&G Sweet Heat Peppers

Progesterone Capsules (Dr. Reddy's) – dissolution failure (2021)

Failed Dissolution Specifications: Out-of-specification results observed for dissolution during stability testing.

Class IIModerate

FDAFeb 26, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Fruit Punch Zero (Electrolit) – Undeclared color (2021)

Undeclared Allergen

Product contains undeclared FD&C Red No. 40.

Class IIILow

FDAFeb 26, 2021AL, AZ, CA +19 more• Laboratorios Pisa Sa De Cv

Ponche Fruit Punch (Electrolit) – Undeclared color (2021)

Undeclared Allergen

Product contains undeclared FD&C Red No. 40.

Class IIILow

FDAFeb 26, 2021AL, AZ, CA +19 more• Laboratorios Pisa Sa De Cv

Imatinib Mesylate Tablets (Dr. Reddy's) – Poisoning Risk (2021)

This recall involves blister packages of prescription medications. The name and strength of the medication, "For Institutional Use only," "Rx Only," lot number and expiration date are printed on the outside of the package as well as on the individual blister units. The Dr. Reddy's logo and NDC number are printed on the outside of the package. The recalled medications include the following: Recalled Prescription Drugs NDC Numbers Carton Configurations Lot Numbers Expiration Dates Imatinib Mesylate Tablets 100 mg 43598-344-31 3 blister cards of 10 tablets H2000138 2022-0630 Imatinib Mesylate Tablets 400 mg 43598-345-31 3 blister cards of 10 tablets H2000127 2022-0630 Pregabalin Capsules 50 mg 43598-292-66 5 blister cards of 10 capsules T900876 2021-0630 Pregabalin Capsules 75 mg 43598-293-66 5 blister cards of 10 capsules T901021 2021-0731 Pregabalin Capsules 100 mg 43598-294-66 5 blister cards of 10 capsules T901022 2021-0731 Pregabalin Capsules 150 mg 43598-295-66 5 blister cards of 10 capsules T901023 2021-0731 Sevelamer Carbonate Tablets 800 mg 55111-789-11 4 blister cards of 25 tablets T801003, T000009, T900221 2020-1031, 2021-1231, 2021-0228 Tadalafil Tablets 5 mg 43598-575-31 3 blister cards of 10 tablets T000376 2022-0131 Tadalafil Tablets 20 mg 43598-573-31 3 blister cards of 10 tablets T000425 2022-0228

CPSCFeb 25, 2021Nationwide• Dr. Reddy's Laboratories, Ltd., of India

BioMedical Equipment Service Co (BMES): Alaris Infusion Pump Module, Model 8100, serviced/repaire...

Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.

FDAFeb 25, 2021CA, IL, IN +6 more• BioMedical Equipment Service Co (BMES)

Mindray DS USA, Inc. dba Mindray North America: Mindray BeneVision Distributed Monitoring System( DMS) 1....

BeneVision DMS may intermittently freeze and require a manual reboot after which normal operation resumes. If a freeze occur, patients monitored on a telemetry transmitter will no longer communicate data to the BeneVision DMS

FDAFeb 22, 2021Nationwide• Mindray DS USA, Inc. dba Mindray North America

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation 4.5, 4.7, 4.9, 5, 6, 7, 8A, 8B, 9A, 9B, 10A, 1...

For some LINAC types, merging clinical beams with beams of approximate dose may lead to the approximate dose erroneously labeled as clinical dose. Merge beams can be used manually, in scripting, or as part of the Automated breast planning feature. In some cases, when merging two beams where the first beam has clinical dose and the second beam has approximate dose, the dose of the resulting beam will be labeled as Clinical, although dose for some of the beam segments is still calculated with the SVD dose engine and it should be labeled Approximate: Mixed dose. The difference between approximate and final Clinical dose is in most cases small, but there can be body sites such as lung where the difference can be significant.

FDAFeb 22, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Methylprednisolone Tablets (Jubilant Cadista) – Illegible Label (2021)

Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.

Class IIILow

FDAFeb 19, 2021Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Atorvastatin Calcium 40mg (Dr. Reddy's) – Impurity Specifications (2021)

Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities

Class IIILow

FDAFeb 19, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Imatinib Mesylate 100mg (Dr. Reddy's) – Dissolution Issue (2021)

Failed Dissolution Specifications

Class IIModerate

FDAFeb 17, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

In2Bones, SAS 28 Chemin du petit Bois Ecully France: In2Bones Shannon Percutaneous Burr - Product Usage: indi...

This Field Action is being conducted following identification of manufacturing non-conformity of some batches of Shannon burrs diameter 2.0mm length 20mm, possibly causing the breakage of the burr during use.

FDAFeb 9, 2021Nationwide• In2Bones, SAS 28 Chemin du petit Bois Ecully France

Panang Curry Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Thai Peanut Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet