laceration risk Recalls

Made Fresh Salads Garlic & Herb Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Products may be contaminated with Listeria monocytogenes.

Mentor Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Merit Medical BioFlo DuraMax Catheter Recall 2026: 47,153 Units Worldwide

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)

Probes may rupture/burst during activation

Oregon Potato Company Recalls Blueberries Due to Listeria Risk

Erbe USA Recalls 5,154 Flexible Cryoprobes for Surgical Use Over Rupture Risk (2026)

Erbe USA recalled 5,154 Flexible Cryoprobes used in surgery after probes may rupture during activation. The defect can cause rupture or burst during activation. Stop using the device and follow recall instructions from the manufacturer.

Fortemotus Bed Rails Recalled Over Entrapment and Asphyxiation Risk

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Products contain undeclared milk and soy.

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

Orthalign Drill Plate Recall 2026 for 7 Units Over Bone-Cut Risk

Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

Orthalign Lantern Knee Drill Plate Recalled for Bone-Cut Risk (2026)

Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

Little Cow Company Recalls 9 oz Glass Jar Candles Over Fire, Burn and Laceration Hazards (2026)

B. Braun Medical Recalls BBraun Medical 21G Winged INF 7B3050 for 105,550 Units (2026)

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

B. Braun Medical 21GA Winged Infusion Set 7M2802 Recalled 51,300 Units (2026)

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

B. Braun Medical Recalls 21GA Winged Infusion Set (7A3842) 21,000 Units (2026)

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.