Daye (Anne's Day Ltd)

Complete recall history across all FDA and CPSC categories — 29 total recalls

Daye (Anne's Day Ltd) appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (29)

FDA medical device enforcement actions by Daye (Anne's Day Ltd)

Date Product Reason Class
Feb 17, 2025 Refill 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-M... Product lacks 510(k) clearance. Class II
Feb 17, 2025 9 Coated Regular Tampons and 9 Nude Regular Tampons; Model Number: FG-TMP-RE... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-M... Product lacks 510(k) clearance. Class II
Feb 17, 2025 9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 All in One Bundle; Model Number: FG-BNDL-PC-REFAIO; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-REF09090909; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 9 Coated Regular and 9 Nude Regular Tampons; Model Number: FG-TMP-REF09000900; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Regular Flow Bundle; Model Number: FG-BNDL-PC-REFRF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 18 Coated Super Tampons; Model Number: FG-TMP-REF00180000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-T... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-T... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-IBHF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 36 Coated Super Tampons; Model Number: FG-TMP-MM-REF00360000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-REFHF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-RE... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Heavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-IBRF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Trial Tampon Box; Model Number: FG-TMP-REF04050504; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 36 Coated Super Tampons; Model Number: FG-TMP-MM-IB00360000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-IBAIO; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909; Product lacks 510(k) clearance. Class II
Feb 17, 2025 9 Coated Super and 9 Nude Super Tampons; Model Number: FG-TMP-REF00090009; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Initiation 36 Coated Regular Tampons; Model Number: FG-TMP-MM-IB36000000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000; Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-REFRF; Product lacks 510(k) clearance. Class II
Feb 17, 2025 9 Coated Super Tampons and 9 Nude Super Tampons; Model Number: FG-TMP-RET000... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-M... Product lacks 510(k) clearance. Class II
Feb 17, 2025 Refill 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-REFAIO; Product lacks 510(k) clearance. Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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