Trinity Care Solutions Recalls Invanz Due to Sterility Concerns
Trinity Care Solutions is recalling 12 units of compounded Invanz in Florida due to quality control concerns regarding sterility assurance identified during an FDA inspection.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a lack of assurance of sterility in a parenteral product, which poses a significant risk of serious health consequences such as infection.
Plain-English summary
Trinity Care Solutions, operating as Franck's Lab Inc, is recalling 12 units of Invanz (ertapenem) 1 gm/100 mL 0.9%NS. The affected products were compounded for parenteral use and distributed in Florida. The recall includes two specific prescription lots: Rx # 29157 with a discard date of 05/19/14, and Rx # 29097 with a discard date of 05/20/14.
The recall was initiated due to a lack of assurance of sterility. This decision follows concerns associated with quality control procedures observed during a recent FDA inspection. The agency has classified this recall as Class II.
Patients who received these specific lots of Invanz should contact their healthcare provider or pharmacist for guidance. The source text does not report any illnesses or injuries associated with the use of these products.
The recalled product
- Product
- Invanz (ertapenem)1 gm/100 mL 0.9%NS, Trinity Care Solutions, 202-C SW 17th Street, Ocala, FL 34471-5138, For Parenteral Use Only, Rx # 29157, Discard After 05/19/14; Rx # 29097, Discard After 05/20/14
- Manufacturer
- Franck's Lab Inc dba Trinity Care Solutions
- Affected units
- 12
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Rx # 29157
- Exp 5/19/14
- Rx # 29097
- Exp 5/20/14
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 30 recalled by Franck's Lab Inc dba Trinity Care Solutions under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 30 products in this recall →Related recalls
Same manufacturer · Franck's Lab Inc dba Trinity Care Solutions
See all →- SevereTrinity Care Solutions Recalls ANA Kit Due to Sterility Concerns
FDA (Drugs) · 2014-07-30
- SevereTrinity Care Solutions Recalls Compounded Cubicin Due to Sterility Concerns
FDA (Drugs) · 2014-07-30
- SevereTrinity Care Solutions Recalls Desferal Sterile Compounds Due to Sterility Concerns
FDA (Drugs) · 2014-07-30
- SevereTrinity Care Solutions Recalls Compounded Cubicin Due to Sterility Concerns
FDA (Drugs) · 2014-07-30
- SevereTrinity Care Solutions Recalls Unasyn Due to Sterility Concerns
FDA (Drugs) · 2014-07-30
Same hazard · sterility
See all →- SevereK.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Tri-MIX Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Tirzepatide Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereK.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
Similar recalls
- SevereSentara Recalls Invanz Injection Homepumps Due to Sterility Concerns
FDA (Drugs) · 2016-02-03
- SevereLincare Recalls TPN 3:1 Bags Due to Sterility Concerns
FDA (Drugs) · 2015-07-08
- HighErtapenem Injectable Antibiotic Bags Recalled for Lack of Sterility Assurance
FDA (Drugs) · 2023-02-22
- SevereWalgreens Recalls Invanz Minibags Due to Sterility Assurance Concerns
FDA (Drugs) · 2016-01-06
- SeverePharm D Solutions Recalls Tri-Mix Injectable Due to Sterility Concerns
FDA (Drugs) · 2018-11-07
- SevereEssential Wellness Pharma Recalls TRIMIX #1 Injection Due to Sterility Concerns
FDA (Drugs) · 2015-11-25