Recall Z-2239-2016— Hologic, Inc
Class II · Terminated
Class II FDA medical device recall by Hologic, Inc, initiated 2016-05-31, terminated 2017-05-24. FDA's recall record names no specific 510(k) clearance for this event. Product: ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast biopsy.. Reason: Cracks ATEC Canister Lids..
- Recalling firm
- Hologic, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-05-31
- Terminated
- 2017-05-24
- Firm location
- Marlborough, MA, United States
Product description
ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast biopsy.
Reason for recall
Cracks ATEC Canister Lids.
Data sourced from openFDA. This site is unofficial and independent of the FDA.