Bausch + Lomb Phaco Pack recall
BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
Why was Bausch + Lomb Phaco Pack recalled?
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN (01) 40193489234405, Lot Number 22DBM505
- Product
- BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 160 kits
- Distribution
- US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.
- Recall date
- November 9, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)