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Gilster-Mary Lee Corp.

Gilster-Mary Lee Corp. Recalls

All product recalls associated with Gilster-Mary Lee Corp..

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Recall Summary

Total Recalls

1000

Past Year

353

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 1541–1560 of 3680 recalls

Organic Unsalted Microwave Popcorn (Gilster-Mary Lee) - Glass Contamination (2020)

Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size

Class IIModerate

FDASep 9, 2020AZ, CA, CT +19 more• Gilster-Mary Lee Corp.

Organic Microwave Popcorn (Gilster-Mary Lee) - Glass Contamination (2020)

Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size

Class IIModerate

FDASep 9, 2020AZ, CA, CT +19 more• Gilster-Mary Lee Corp.

Lightly Salted Microwave Popcorn (Gilster-Mary Lee) - Glass Contamination (2020)

Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size

Class II

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Moderate

FDASep 9, 2020AZ, CA, CT +19 more• Gilster-Mary Lee Corp.

AESCULAP S4 Cervical Cross Connector (Aesculap) - Clamping force issue (2020)

Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.

FDASep 8, 2020Nationwide• Aesculap Implant Systems LLC

2020 Utilimaster Metris (Utilimaster) - Payload label error (2020)

Shyft Group is recalling certain 2020 Fleet Vehicles-Utilimaster Metris vehicles. The payload capacity shown on the Tire and Loading Information label may be higher than the actual payload capacity of the vehicle.

NHTSASep 2, 2020Nationwide• UTILIMASTER

Terumo Perfusion System (Terumo) – Air Sensor Connector Risk (2020)

Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.

FDAAug 25, 2020Nationwide• Terumo Cardiovascular Systems Corporation

SOBEL WESTEX Disposable Isolation Gown Made in China RN#7... – due to non-surgical isolation gowns n... (2020)

Due to non-surgical isolation gowns not meeting all performance test requirements.

FDAAug 13, 2020Nationwide• Sobel Westex

Red Onions (Lancaster Foods) – Contamination Potential (2020)

Salmonella

Lancaster Foods LLC, 7700 Conowingo Avenue, Jessup, MD 20794 is initiating a recall of products that may have been made with the 500 pounds (bulk) of red onions out of a lot of 12,000 pounds (bulk) that were under the recalled Thomson International lots because of potential presence of salmonella bacteria. Lancaster Foods LLC. states that all minimally processed items go through a sanitize step of chlorine dioxide.

Class IHigh

FDAAug 10, 2020AR, CT, DE +4 more• Lancaster Foods LLC

Plastic Cannula (Greiner) – sample leakage (2020)

Sample leaking from the sleeve covering the needle inside the cannula

FDAJul 27, 2020Nationwide• C.A. Greiner & Sohne Gesellschaftmbh Greiner St. # 70 Kremsmunster Austria

DABRA Excimer Laser (Ra Medical) – mounting stability (2020)

Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.

FDAJul 24, 2020Nationwide• Ra Medical Systems, Inc.

CombiDiagnost R90 (Philips) – software value lock (2020)

Philips has become aware of a software issue, where the kV and mA values are not locked immediately but change when the collimator shutter position is changed directly after the Lock-In command. This software issue leads to an over or under exposed image.

FDAJul 22, 2020Nationwide• Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany

Lobster Meat (Greenhead) – Listeria Risk (2020)

Listeria

Ready-to-eat lobster meat may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 16, 2020CO, CT, ME +2 more• Greenhead Lobster Products

ENNOVATE MIS Removal Key (Aesculap) - Instrument Fracture Risk (2020)

Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system.

FDAJul 13, 2020Nationwide• Aesculap Implant Systems LLC

Ultimax-i X-Ray System (Canon Medical) - Image Transfer Fault (2020)

During a procedure, when images were acquired, and these images were transferred to PACS /image archival system, the number of images displayed were not the same as originally acquired.

FDAJul 8, 2020CA, CT, ID +7 more• Canon Medical System, USA, INC.

Raspberry Zingers (Hostess) – Potential Mold (2020)

Product potentially has mold prior to best by date.

Class IIModerate

FDAJul 2, 2020Nationwide• Hostess Brands, LLC