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Jiangsu Shenli Medical Production Co., Ltd. No.

Jiangsu Shenli Medical Production Co., Ltd. No. Recalls

All product recalls associated with Jiangsu Shenli Medical Production Co., Ltd. No..

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Recall Summary

Total Recalls

1000

Past Year

1000

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 2501–2520 of 21320 recalls

100 mL Luer Lock Syringe (Medigrative) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

WishFIX Growth Plating System (Wishbone) – Implant Mislabeling (2024)

The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.

Low

FDAApr 5, 2024CT, FL, NJ• Wishbone Medical, Inc.

Blues Hog Sweet & Savory Seasoning – Undeclared Allergens (2024)

Undeclared Gluten

Undeclared wheat, soy flour and soy lecithin

Class IIILow

1...124 125126127 128...1066

Page 126 of 1066Next

FDA

Apr 5, 2024

• Baron Spices Inc

IntelliSpace Cardiovascular Software (Philips) – Data Export Issue (2024)

Study data is not able to be archived, copied, or exported with the cardiovascular software version.

Low

FDAApr 4, 2024Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Mainstays Electric Mini Choppers – Laceration Risk (2024)

Laceration Risk

This recall involves Mainstays Electric Mini Choppers with model number MS14100094536S1. The choppers are rechargeable and cordless, and have a green lid, white body, and clear plastic bowl. They have one blade attachment, which consists of three curved blades on one white plastic spindle. Model number MS14100094536S1 is on the label attached to the bottom of the clear plastic bowl.

High

CPSCApr 4, 2024Nationwide• Shuangma Plastic Manufacturing Inc., of China

InstaClear Lens Sheath (Olympus) – Potential Breakage (2024)

Potential for distal end of the sheath to break off during a procedure.

Moderate

FDAApr 3, 2024Nationwide• Olympus Corporation of the Americas

Airvo 2 Humidifier (Fisher & Paykel) – Speaker Configuration (2024)

Humidifier devices, used to deliver high flow respiratory therapy to patients, manufactured before 14 August 2017, have a speaker configuration that may result in distorted, intermittent or inaudible alarm sound levels. In the absence of an audible alarm, if there is an interruption to therapy, a patient may experience oxygen desaturation.

Moderate

FDAApr 2, 2024Nationwide• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

Cyclophosphamide 1g Injection (X-Gen) – Labeling Error (2024)

Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.

Class IIILow

FDAApr 2, 2024Nationwide• X-Gen Pharmaceuticals Inc.

Cyclophosphamide 500mg Injection (X-Gen) – Labeling Error (2024)

Class IIILow

FDAApr 2, 2024Nationwide• X-Gen Pharmaceuticals Inc.

EchoTip Ultrasound Needle (Cook) – Bacterial Endotoxin Levels (2024)

Devices may contain elevated levels of bacterial endotoxin.

Low

FDAApr 1, 2024IN• Cook Medical Incorporated

EchoTip Ultrasound Needle (Cook) – Bacterial Endotoxin Levels (2024)

Devices may contain elevated levels of bacterial endotoxin.

Low

FDAApr 1, 2024IN• Cook Medical Incorporated

OmniLab Advanced+ Ventilator (Philips) – Therapy Interruption Risk (2024)

Device may experience an interruption or loss of therapy in case of a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death.

High

FDAApr 1, 2024Nationwide• Philips Respironics, Inc.

LOSPA Patella Component (Corentec) – Expiration Date Issue (2024)

Due to unsupported 10 year expiration date.

Low

FDAMar 29, 2024Nationwide• CORENTEC CO., LTD 12 Yeongsanhong1-Gil; Seobuk Cheonan Korea (the Republic of)

LOSPA Tibial Insert (Corentec) – Expiration Date Issue (2024)

Due to unsupported 10 year expiration date.

Low

FDAMar 29, 2024Nationwide• CORENTEC CO., LTD 12 Yeongsanhong1-Gil; Seobuk Cheonan Korea (the Republic of)

Spectral CT Oncology Package (Philips) – Laser Marking Risk (2024)

Potential for third party oncology marking laser to be reflected off the gantry cover surface, which can potentially lead to misdiagnosis and subsequent incorrect treatment.

Moderate

FDAMar 29, 2024Nationwide• Philips North America Llc

Helados Mexico Ice Cream Minis (Tropicale Foods) – Salmonella Risk (2024)

Salmonella

Salmonella contamination

Class IHigh

FDAMar 29, 2024IL, KY, MI +3 more• Tropicale Foods, Inc.

Intellis AdaptiveStim (Medtronic) – Reprogramming Limitation (2024)

inability to reprogram one device

Moderate

FDAMar 28, 2024IN• Medtronic Neuromodulation

G5 Transit Bus (Micro Bird) – Defroster System Failure (2024)

Corp. Micro Bird, Inc. (Micro Bird) is recalling one 2019 G5 bus. A LIN gateway module may fail causing the defrosting system to be inoperative. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 103, "Windshield Defrosting and Defogging Systems."

High

NHTSAMar 28, 2024Nationwide• MICRO BIRD

G5 School Bus (Micro Bird) – Defroster System Failure (2024)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2019 G5 school buses. A LIN gateway module may fail causing the defrosting system to be inoperative. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 103, "Windshield Defrosting and Defogging Systems."

High

NHTSAMar 28, 2024Nationwide• MICRO BIRD

Isotretinoin 40mg Capsules (Teva) – Superpotent Drug (2024)

Superpotent Drug: The 3-month stability result for assay was found to be above specification limit

Class IIModerate

FDAMar 28, 2024Nationwide• Teva Pharmaceuticals USA, Inc