CooperSurgical, Inc.: 40 recalls on record

Recalls filed with 1 agency: FDA (40).

First recall on record: December 5, 2012. Most recent: December 25, 2024.

Risk classification: Class I: 1 · Class II: 27 · Class III: 12

Most recent recalls

DateAgencyProduct
December 25, 2024FDABrand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unk…Z-0692-2025
December 25, 2024FDABrand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065…Z-0687-2025
December 25, 2024FDABrand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23054 Sof…Z-0689-2025
December 25, 2024FDABrand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 So…Z-0688-2025
December 25, 2024FDABrand Name: K-Systems Product Name: R65 Trolley Model/Catalog Number: K24012 Software …Z-0691-2025
December 25, 2024FDABrand Name: K-Systems Product Name: T47 Warming Plate Model/Catalog Number: K23055 Sof…Z-0690-2025
October 2, 2024FDAOrigio Sperm Wash Medium Pack of Ten 10ml bottles - Intended for washing of spermatozoa …Z-3296-2024
October 2, 2024FDAStainless Steel Sims Uterine Sound, Part Number 64-601Z-3189-2024
October 2, 2024FDASilver-Plated Copper Sims Uterine Sound, Part Number 64-600Z-3188-2024
October 2, 2024FDAOrigio Sperm Wash Medium Pack of Five 60ml bottles - Intended for washing of spermatozoa.…Z-3297-2024
October 2, 2024FDAOrigio Sperm Wash Medium Pack of Five 60ml bottles - Intended for washing of spermatozoa.…Z-3298-2024
February 21, 2024FDAglobal Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (10…Z-1089-2024
February 14, 2024FDABox as labeled: Regard, Carter-Thomason CloseSure System XL, REF 733776, Quantity 1 Box o…Z-0985-2024
February 23, 2022FDAPARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an in…D-0643-2022
November 24, 2021FDAQuantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075Z-0261-2022
July 15, 2020FDACOOPERSURGICAL Os FinderTM Cervical Dilator, Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm…Z-2498-2020
December 11, 2019FDAQuantam 2000 Electrosurgical Generator, Part number 909075-05W.Z-0602-2020
October 17, 2018FDAColpo-Pneumo Occluder, Part CPO-6Z-0098-2019
October 3, 2018FDARetractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Re…Z-3278-2018
March 16, 2016FDAMilex Arcing Diaphragm Size 95; Model Number: MXWS95Z-1054-2016
March 25, 2015FDAMediChoice WarmGel Infant Heel Warmer, Item # 1643069911 MediChoice Liquid Infant Heel …Z-1300-2015
December 10, 2014FDACooper Surgical CANNULA-CURETTE 12MM; Model Number: MX562 The CooperSurgical SUCTION C…Z-0488-2015
December 3, 2014FDACooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5…Z-0484-2015
November 19, 2014FDACooperSurgical MILEX PESSARY KITS- Hodge w/Support Folding Pessary- #1 Model: MXKPHS01 …Z-0208-2015
November 19, 2014FDACooperSurgical MILEX PESSARY KITS-Ring w/Support Folding Pessary- #1 Model: MXKPRS01 …Z-0207-2015

Questions about this company

How many recalls does CooperSurgical, Inc. have?
Recalert has 40 U.S. recalls on record for CooperSurgical, Inc., published between December 5, 2012 and December 25, 2024.
What was the most recent CooperSurgical, Inc. recall?
FDA recall Z-0692-2025, published December 25, 2024: Brand Name: K-Systems Product Name: Multiple/unknown Model/Catalog Number: Multiple/unknown Software Version: N/A Product Description: An electrically-powered device intended to provide suitable …
Which agencies have handled CooperSurgical, Inc. recalls?
CooperSurgical, Inc. appears as the recalling firm in recalls from: FDA (40).

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