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Penn Herb Company, Ltd.

Penn Herb Company, Ltd. Recalls

All product recalls associated with Penn Herb Company, Ltd..

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 1401–1420 of 17592 recalls

Thyroid Formula Capsules (Penn Herb) – Salmonella risk (2024)

Salmonella

Potential Salmonella contamination

Class IHigh

FDAJun 3, 2024CA, FL, IL +7 more• Penn Herb Company, Ltd.

Bottle Decanter (Microtek Medical) – Packaging Integrity Issue (2024)

During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.

Moderate

FDAJun 3, 2024Nationwide• Microtek Medical Inc.

Vial Decanter (Microtek Medical) – Packaging Integrity Issue (2024)

During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.

Moderate

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FDA

Jun 3, 2024

Nationwide

• Microtek Medical Inc.

Nanoplasty Bunion Correction System (Treace Medical) – Screw Interference (2024)

Potential issue causing a higher frequency of interference with locking screws and/or inserter rods than anticipated, resulting in screws stripping and/or not fully seating in the plates and/or interface issues between inserter rods and plates.

Moderate

FDAJun 2, 2024Nationwide• Treace Medical Concepts, Inc.

Soltive Premium Laser System (Olympus) – Footswitch Pairing Issue (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

Moderate

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

Soltive Pro Laser System (Olympus) – Footswitch Pairing Issue (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

Moderate

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

Soltive Laser Wireless Footswitch (Olympus) – Pairing Problem (2024)

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

Moderate

FDAMay 31, 2024Nationwide• Olympus Corporation of the Americas

ABL800 FLEX Analyzer (Radiometer) – Calibration Solution Issue (2024)

Issue with analyzer when the pH of the calibration solution decreases during the in-use period potentially because of bacterial growth in the calibration solution bottles. This may result in a probability of reporting biased out-of-specification pH results on blood samples.

Moderate

FDAMay 31, 2024Nationwide• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

Super Vinegar Cleaner (Compare Brands) – poisoning risk (2024)

Fire/Burn Risk

This recall involves the ADIOS! Super Vinegar All Natural Cleaner, 30%. The cleaner's bottles are labeled on the front with: "ADIOS! SUPER VINEGAR ALL NATURAL CLEANER. 30% Concentrate Indoor & Outdoor use". There is a label on the back with: "Say ADIOS to industrial cleaners with the natural power of vinegar" along with safety information and instructions. The product was sold in a 16 oz. white bottle with a blue cap.

High

CPSCMay 30, 2024Nationwide• Compare Brands LLC, of Fort Wayne, Indiana

Colby Jack Cheese Slices (Tillamook) – plastic material (2024)

Plastic material. The piece of plastic material was detected in a 40lb. cheese block and smaller fragments of the plastic material may be found in the cheese slices.

Class IIModerate

FDAMay 30, 2024IN, UT, WA• Tillamook County Creamery Association

Petroleum Jelly (Consumer Product) – Labeling Error (2024)

Labeling: Label Mix up; product labeled as pure white petroleum jelly actually contains petroleum jelly with Lavendar and Chamomile

Class IIModerate

FDAMay 28, 2024Nationwide• Consumer Product Partners, LLC

PROBEAT-FR (Hitachi) – Image Matching Software Error (2024)

During positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are insufficient in number.

Low

FDAMay 27, 2024Nationwide• Hitachi America, Ltd., Particle Therapy Division

Beckman Coulter IGM Reagent (Beckman Coulter) – Lipemia Result Inaccuracy (2024)

LIH Influence check settings for Lipemia are incorrect which may result patient samples being reported as false low results or cause a high result to report as normal

Moderate

FDAMay 27, 2024Nationwide• Beckman Coulter Inc.

WOM Tube Set (WOM) – Transponder Data Error (2024)

Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery

Low

FDAMay 24, 2024Nationwide• WOM World Of Medicine AG Alte Poststr. 11 Ludwigsstadt Germany

CentriMag Primary Console (Thoratec) – Power Standard Nonconformance (2024)

Due to a component change, the console part of a circulatory support system may not conform to the IEC 61000-4-5 standard, so if subjected to a power surge above 1.8kV and up to 2.0 kV, the console may shut down completely without alarm, pumping would cease, and the patient would have to be switched to a backup circulatory support system.

High

FDAMay 22, 2024Nationwide• Thoratec Switzerland GMBH Technoparkstrasse 1 Zurich Switzerland

Endo Model M Tibial Components (Waldemar Link) – Surgical Screw Issue (2024)

Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

High

FDAMay 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

DxI 9000 Access Analyzer (Beckman Coulter) – Laboratory System Compatibility (2024)

When a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory Automation System (LAS) and is running with the system software versions 1.17.0 and below, the analyzer does not send a message to the LAS when the sample wheel is full, and the LAS continues sending samples despite the limited capacity to process new samples. Therefore, sample tests may be aliquoted but not processed when the number of tests associated with onboard patient samples exceeds the throughput limit. If this issue occurs test results are flagged with a sample wheel timeout (SWT) error flag, and there may be a delay in reporting test results which could lead to a delay in patient treatment.

Moderate

FDAMay 22, 2024Nationwide• Beckman Coulter, Inc.

Endo Model SL Tibial Components (Waldemar Link) – Surgical Screw Problem (2024)

Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

High

FDAMay 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Prelude Roadster Guide Sheath (Merit Medical) – Connection Risk (2024)

Due to older version of Instruction for Use (IFU) instructing to ensure that the value and the sheath are tightly connected before use. This may cause users to over-tightening the luer which may result in the swivel nut detaching from the HVA body.

Moderate

FDAMay 22, 2024Nationwide• Merit Medical Systems, Inc.

Beckman Coulter DxI 9000 Analyzer (Beckman Coulter) – System Connectivity (2024)

The reason for this recall is Beckman Coulter has determined that when a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory Automation System (LAS); is running with the software versions 1.17 and below; and a sample tube is sent from the LAS to DxI 9000 Access Immunoassay Analyzer, an out of sequence message will be sent from the Analyzer to the LAS. This issue may result in multiple error messages (i.e., a sample pick and place (PnP) error or a no result obtained (NRT) flag may be displayed) and subsequently a risk of delays in processing/reporting patient test results and patient treatment.

Moderate

FDAMay 22, 2024Nationwide• Beckman Coulter, Inc.