🏥 Medical Devices Class I - Dangerous
The syringe carrier is missing components: a damper and spring.
All Recalls
95,114 total recalls in our database
Bio-MAC Cannula (Needle) Set
Biologic Therapies
🏥 Medical Devices Class I - Dangerous
Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution
🏥 Medical Devices Class I - Dangerous
Specific Aespire 7900 Anesthesia Machines have an increased likelihood of failure of the CPU circuit board. This could result in a blank display or loss of mechanical ventilation.
RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical instrument for hip implantation.
DePuy Orthopaedics
🏥 Medical Devices Class I - Dangerous
This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may fracture during surgery and there is the potential for plastic pieces to be left in the patient.
🏥 Medical Devices Class I - Dangerous
The firm is recalling ToggleLocs and Ziploops manufactured in May and July of 2014 as they were not processed following a standard work process, which resulted in complaints of sterile packaging not being sealed.
🏥 Medical Devices Class I - Dangerous
The firm is recalling ToggleLocs and Ziploops manufactured in May and July of 2014 as they were not processed following a standard work process, which resulted in complaints of sterile packaging not being sealed.
ACCU-CHEK Connect Diabetes Management App; Instruction Manual Designed to transfer data for diabetes management.
Roche Diabetes Care
🏥 Medical Devices Class I - Dangerous
Roche Diabetes Care has become aware of an issue with the Accu-Chek Connect diabetes management app that could potentially lead to inaccurate bolus advice being provided to the user. A thorough investigation of the situation revealed that this issue may occur if the user changes the screen orientation of the phone from portrait to landscape or vise versa while looking at the Bolus Advisor or Carb
🏥 Medical Devices Class I - Dangerous
Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Referencing Sizer with Locking Boom, part number 42-5099-088-10. Devices are being removed from distribution due to nonconforming to print specifications.
Skintact ECG Electrode FS-50, Catalog no. 58028 , & Stable Base ECG Electrode SBT-60, Catalog no. 50547. To acquire and transmit the electrical signal at the body surface to a processor that produces an electrocardiogram (ECG) or vectorcardiogram.
Leonhard Lang Medizintechnik GmbH
🏥 Medical Devices Class I - Dangerous
The electrodes may fail to transmit signals.
Product is mislabeled as Double Swivel Connector with Suction Port and is actually Double Swivel Connector without Suction port. If the incorrect component is not identified prior to clinical use, the incorrect connector would be replaced during the case without risk to the patient and could result in a short delay of the procedure.
🏥 Medical Devices Class I - Dangerous
This recall is being conducted because a cohesive band used to package the devices contains latex and the product is not labeled as required by 21 CFR 801.437; it does not contain Caution: The Packaging of This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
🏥 Medical Devices Class I - Dangerous
This recall is being conducted because a cohesive band used to package the devices contains latex and the product is not labeled as required by 21 CFR 801.437; it does not contain Caution: The Packaging of This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
🏥 Medical Devices Class I - Dangerous
Medcomp has initiated the recall of Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split Cath III, PC Split Cath III because the product shipped was out of specification. One BI (biological indicator) out of 21 on the sterilization load was out of specification.
Children's Pajamas
Unknown Manufacturer
🏠 Consumer Products Class II - Moderate
The pajamas fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Patio set rockers
Guangdong Shunde Baiming Industry Co., Ltd., of China
🏠 Consumer Products Class II - Moderate
The patio sets' rocking chairs can break during normal use, posing a fall hazard to consumers.
🍎 Food Class I - Dangerous
Aloha has recalled protein powder dietary supplements due to the presence of Staphylococcus enterotoxin
Reo Ranch House Sizzling Steak Beef Jerky Seasoning Total Net Wt. 7.74 LBS Reo Spice & Seasoning, INC. Huntsville, TX 77320 (936)294-0222
Reo Spice & Seasoning
🍎 Food Class I - Dangerous
Product may contain undeclared peanuts.
🍎 Food Class I - Dangerous
Undeclared Peanuts.
🍎 Food Class I - Dangerous
Unilever United States, Inc. is voluntarily recalling a limited number of tubs of Breyers¿ No Sugar Added Salted Caramel Swirl because they may inadvertently contain almonds, which are not listed as an ingredient on the label.
🍎 Food Class I - Dangerous
The products were shipped without labels declaring the nutrition and ingredients information and the presence of egg, milk, and wheat allergens.