Cardinal Health Inc. recalls LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile,…
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Read the official notice →- Date
- 2023-11-29
- Country
- United States
- Brand
- Cardinal Health
- Product
- LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile,…
- Classification
- Class I
- Units
- Nationwide in the USA
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Cardinal Health recalls
- 2024-02-14
USCardinal Health 200, LLC recalls Cardinal Health Monoject, 1 mL Purple Enteral Syringe with Enfit Connection Sterile, REF 401SE
Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35, and 60 mL) and Cardinal Health…
FDA · DeviceCardinal Health 200, LLCDistribution US nationwide and Canada. Foreign distribution updated 9/6/2024…Official notice →- US
Cardinal Health 200, LLC recalls Cardinal Health Monoject, 35mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF 435SE
The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility issues with certain syringe enteral feeding pumps. As a result, Cardinal Health recommends…
FDA · DeviceCardinal Health 200, LLCDistribution US nationwide and Canada. Foreign distribution updated 9/6/2024…Official notice → - 2024-01-24
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Cardinal Health 200, LLC recalls CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510
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- 2023-11-01
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FDA · DeviceCardinal Health 200, LLCNationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL,…Official notice → - 2023-10-18
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Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip,…
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FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
Other drugs & medical recalls in the United States
- 2023-11-29
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Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…
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- US
- US
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