Recall Register

Food, drugs, devices › Firms

Magellan Diagnostics, Inc.

FDA recalling firm · 9 enforcement events · 16 product records · 2014–2026 · MA

Magellan Diagnostics, Inc. has 9 FDA enforcement events on this register (16 product records) between 2014 and 2026: 9 device; the busiest year was 2018 with 2.

33% of its events are Class I; the most common class is Class II (6). 3 events are listed as ongoing; the recalling firm's address is in MA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
13 Mar 2026(1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, (4)LeadCare¿ II 9X Blood Lead Test Kit ; Catalog Number(s): (1) 70-6762, (2) 70-6762RUO, (3) 70-8404 (Box containing 5 Test Kits), (4) 70-9000 (Box containing 9 test kits); The LeadCare II kit is provided with the following materials: "…DeviceClass II3Ongoing
23 Feb 2024The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packages of 24 tubes each; 48 tests) "…DeviceClass II1Ongoing
19 Sep 2023LeadCare II Blood Lead Test Kit-For in vitro diagnostic use only. The test kit is for the quantitative measurement of lead in capillary whole blood.DeviceClass II1Ongoing
7 May 2021LeadCare II Blood Lead Test Kit Catalog Number 70-6762DeviceClass I3Terminated
8 Aug 2018Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test for the measurement of lead in fresh whole blood. Catalog Number: 70-6762 Primary DI No: 00850355006000 The LeadCare II Blood Lead Test Kit is for in vitro diagnostic use only. The test kit is for the quantitative measurement of lead in fresh whole blood. This…DeviceClass II1Terminated
9 Jan 2018LeadCare II Blood Lead Analyzer Part Numbers: 70-6760, 70-6529-R, 70-6760-P, 70-6760-R. Intended for in vitro (external) use only.DeviceClass II2Terminated
23 May 2017Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage: The LeadCare Blood Lead Test Kit is for in vitro diagnostic use only. The Test Kit is for the quantitative measurement of lead in fresh whole blood. This product is for professional use only. Sensors and Treatment Reagent of the Test Kit are…DeviceClass I2Terminated
20 Jan 2016LeadCare II Blood Lead Test Kit, containing LeadCare II Lead Controls Product Usage: IVD test kit for the detection of lead in blood. The kit consists of sensors, treatment reagent, lead controls (two levels), heparinized capillary tubes and plungers, transfer droppers and a calibration button. The LeadCare II Lead…DeviceClass II1Terminated
29 Nov 2014Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010DeviceClass I2Terminated

By type and class

Device9
Class II6
Class I3

Class I: 33% of this firm's events; 18% of all events on the register.

Events by year

14
16
18
20
22
24
26
Enforcement events for Magellan Diagnostics, Inc. by year initiated.

Questions and answers

How many FDA recalls has Magellan Diagnostics, Inc. had?

9 enforcement events (16 product records) on this register, 2014–2026: 9 device.

Are any Magellan Diagnostics, Inc. recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are Magellan Diagnostics, Inc. recalls?

6 Class II, 3 Class I. 33% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.