Severity 2 of 5
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Organic mandarins are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.
Erin's Faces Mineral SPF 32 sunscreen is being recalled because of cGMP deviations. 54 tubes are affected.
Organic lemons are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.
Organic asparagus is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Canturio Smart Extension CSE Implants are being recalled due to a labeling error, with the product incorrectly labeled. 106 units are affected.
Curly parsley and Italian parsley, including organic Italian parsley, are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.
Organic brussels sprouts are being recalled because they may be contaminated with fluid from a reach truck. The source does not state a quantity.
Organic bunched cilantro is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Organic collard greens are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
The Hummingbird Stimulated EMG Kit is being recalled because the product packaging contains the wrong part number and kit contents. 10 units are affected.
Mighties organic kiwi is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Organic spinach is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Organic bunched dill is being recalled because it may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Organic celery products, including sleeved celery, naked celery and celery hearts, are being recalled because they may be contaminated with fluid from a reach truck. 213 cases in total.
Organic bok choy and organic baby bok choy are being recalled because they may be contaminated with fluid from a reach truck. The action covers 213 cases in total.
Philips Ultrasound, Inc. is recalling Philips C5-2 Transducers because they were refurbished beyond their useful life. The affected devices were distributed domestically nationwide and internationally across 49 countries.
ADVIA 120/2120/2120i SETpoint Calibrator lots are being recalled because they have the incorrect platelet value assignments for ADVIA hematology systems. 2,020 units are affected.
Gabapentin Capsules 100 mg from Major Pharmaceuticals are being recalled because of a defective container: the blister packaging was inadequately sealed. 3,527 bags are affected.
Pitavastatin Tablets 1 mg manufactured by Orient Pharma for Teva Pharmaceuticals are being recalled because they failed impurities and degradation specifications. 20,618 bottles affected.
Philips V6-2 Transducers are being recalled because the ultrasound transducer devices were refurbished beyond their useful life. 5,230 units are affected.
BD FACS 7-Color Setup Beads are being recalled because errors in the spectral overlap factors table may affect accurate setup of the flow cytometry instrument. 590 units affected.
Change Healthcare is recalling Cardiology Hemo Software (version 14.3.2 and 15.0.1) because a software update may cause the system to unexpectedly shut down. The recall affects 29 systems distributed across multiple US states and international locations.
ARTIS angiography systems are being recalled because a communication failure between the dose sensor and the software may cause the system to incorrectly report a high dose.