Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Plastikon Healthcare LLC

Plastikon Healthcare LLC Recalls

All product recalls associated with Plastikon Healthcare LLC.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

590

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 2561–2580 of 10391 recalls

Magnesium Aluminum Simethicone MAX (Plastikon Healthcare) – Manufacturing Quality Issue (2022)

CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.

Class IIModerate

FDAJun 7, 2022Nationwide• Plastikon Healthcare LLC

Diphenhydramine HCl Oral Solution (Plastikon Healthcare) – Manufacturing Quality Issue (2022)

CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.

Class IIModerate

FDAJun 7, 2022Nationwide• Plastikon Healthcare LLC

Guaifenesin Dextromethorphan Solution (Plastikon Healthcare) – Manufacturing Quality Issue (2022)

CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.

1...127 128129130 131...520

Page 129 of 520Next

Class IIModerate

FDAJun 7, 2022Nationwide• Plastikon Healthcare LLC

Milk of Magnesia USP (Plastikon Healthcare) – Microbial Contamination (2022)

Microbial Contamination of Non-Sterile Products

Class IHigh

FDAJun 7, 2022Nationwide• Plastikon Healthcare LLC

DVR Anatomic Plate (Changzhou Biomet) – Incorrect Plate Etching (2022)

One lot of DVRASL plates were incorrectly etched and may have been placed into kits as DVRAR or DVRASR plates

FDAJun 2, 2022Nationwide• CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. No. 235 Longhutangjieban Chuangxindadao Xinbei Changzhou China

CT/PET/NM Table (GE Healthcare) – Potential Table Drop (2022)

As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the appropriate table supports in place resulting in injury to service personnel.

FDAJun 2, 2022Nationwide• GE Healthcare, LLC

INFINITY Resect Guide (Wright Medical) – Incorrect Color Coding (2022)

The instrument is incorrectly color coded.

FDAJun 2, 2022Nationwide• Wright Medical Technology, Inc.

RayStation 9B SP1 (RaySearch) – Treatment Course Propagation Problem (2022)

An issue with propagation of treatment course information from RayStation with RayTreat to RayCare has been identified. During some workflows, information may not be propagated to RayCare.

FDAJun 1, 2022Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Aisys CS2 Anesthesia System (GE Healthcare) – Gas Cylinder Transducer Reversal (2022)

There is a potential reversal of the O2 and air cylinder pressure transducer connections.

FDAJun 1, 2022Nationwide• GE Healthcare, LLC

epoc BGEM Test Card (Siemens) – Potential Oxygen Result Bias (2022)

Discrepant (low bias) pO2 results, could be an incorrect diagnosis of hypoxemia and initiation of unnecessary or inappropriate respiratory support.

FDAJun 1, 2022AL, CA, CO +7 more• Siemens Healthcare Diagnostics Inc

Xhibit Telemetry Receiver (Spacelabs) – Alarm Escalation Defect (2022)

Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure.

FDAMay 31, 2022Nationwide• Spacelabs Healthcare, Inc.

NaviCare Nurse Call (Baxter) – Wireless Integration Issue (2022)

An issue has been identified with Phillips (Emergin) and Longleaf non relay (Connexall, Vocera, Cerner) wireless integrations used with NaviCare/Voalte Nurse Call, software versions 3.9.100 through 3.9.300. Calls placed from a push button call device, such as a push button switch, call cord, or from the push buttons on a room audio station, will be canceled on the nurse call system when the call is answered at the wireless phone, regardless of the call priority.

FDAMay 31, 2022Nationwide• Baxter Healthcare Corporation

Thistle Tropical Limeade Juice (Thistle Health) – Hepatitis Risk (2022)

Manufactured using organic strawberries potentially contaminated with Hep A.

Class IIModerate

FDAMay 31, 2022CA, NV, OR +1 more• THISTLE HEALTH INC

Thistle Watermelon Berry Juice (Thistle Health) – Hepatitis Risk (2022)

Manufactured using organic strawberries potentially contaminated with Hep A.

Class IIModerate

FDAMay 31, 2022CA, NV, OR +1 more• THISTLE HEALTH INC

Avance CS2 Anesthesia System (GE Healthcare) – Base Crack Risk (2022)

The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.

FDAMay 27, 2022AZ, CA, CO +25 more• GE Healthcare, LLC

S-Series (Oshkosh) – Alternator Cable Clamp Problem (2022)

Fire/Burn Risk

Oshkosh Corporation (Oshkosh) is recalling certain 2019-2022 S-Series 2.0 Concrete Mixers. Incorrectly installed alternator electrical cable clamps may rub against the vehicle frame or hydraulic hose, possibly damaging the alternator cables.

NHTSAMay 26, 2022Nationwide• OSHKOSH