FDA Device recall Z-0948-2021
REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
- FDA Device
- Class II
- terminated
- Published 2021-02-10
On 2021-02-10 the FDA classified a Class II recall of REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile by Allergan, citing missing Instruction For Use insert.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0948-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-12-29 |
| Published | 2021-02-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Allergan |
| Distribution | MO |
Product
REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
Reason
Missing Instruction For Use insert.
Identifiers
| code_info | Model Number: 91822US UDI Code: (01)00300231822120(17)230705(10)T0464A Lot Number: T0464A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Allergan
- Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie company Madison, NJ…
FDA Drug · Class II · 2021-01-27 · Allergan - Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 Oz bottle, Distributed in the U.S.A. by Allergan, Irvine, CA 92612, NDC 0023-4…
FDA Drug · Class III · 2020-08-05 · Allergan - Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz
FDA Drug · Class III · 2020-08-05 · Allergan - Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40, Style 45 Style 10/UDI:…
FDA Device · Class III · 2019-12-25 · Allergan - NATRELLE Resterilizable Sizers for the styles and sizes: Style 15, Style 20, Inspira X (responsive gel), Inspira F (responsive gel), Inspir…
FDA Device · Class III · 2019-12-25 · Allergan
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0948-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.