Is Chloride recalled?

Yes — there is an active recall. 326 ongoing FDA recalls mention Chloride (1,994 total). Check the affected lots below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloride. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.

Class III · Low risk Terminated Jul 28, 2015

Hydralazine Hydrochloride Injection, USP, 20 mg/mL, 1 mL fill, in a 2 mL; single dose vial. Manufactured by Fresenius Kabi USA…

Reason Incorrect Expiration Date: The "11/06" expiration date printed on the tray (secondary packaging) is incorrect (it should be 11/2016)

Fresenius Kabi USA, LLC NDC 63323-614-01 D-1327-2015

Class III · Low risk Terminated Jul 21, 2015

Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex…

Reason Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.

Apotex Inc. NDC 60505-2742-5 D1834-2015

Class II · Moderate risk Terminated Jul 21, 2015

Ropivacaine HCl 0.2% in 100 mL total volume in a 100 mL Yellow Cassette Res. Flowstop in Sodium Chloride 0.9%, Rx Only…

Reason Lack of Assurance of Sterility: The firm received a complaint of a sterility failure using a non-validated sterility test on a medication cassette.

Pharmedium Services, LLC NDC 61553-834-48 D-1428-2015

Class III · Low risk Terminated Jul 21, 2015

Phentermine Hydrochloride Capsules, USP, 15 mg, packaged in a) 7-count (NDC 55289-791-07), b) 14-count (NDC 55289-791-14), c)…

Reason Failed impurities/Degradation specifications: out of specification results for individual unknown and total impurity at the 12th month room…

PD-Rx Pharmaceuticals, Inc. NDC 55289-791-07 D-0574-2016

Class III · Low risk Terminated Jul 17, 2015

buPROPion Hydrochloride Extended-¿release Tablets USP (SR), 200 mg, Twice-A-Day, Rx Only, 60 count Bottle, Distributed by: Sun…

Reason Failed Dissolution Specification: During analysis of the 18 month long term stability testing, it was noticed that the drug release results at the 4…

Sun Pharma Global Fze NDC 47335-738-86 D-1345-2015

Class I · High risk Terminated Jul 17, 2015

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield…

Reason Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Baxter Healthcare Corp. NDC 0338-0049-11 D-1336-2015

Class I · High risk Terminated Jul 17, 2015

0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare…

Reason Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Baxter Healthcare Corp. NDC 0338-0553-18 D-1335-2015

Class I · High risk Terminated Jul 17, 2015

fentaNYL Citrate, 10 mcg per 1 mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx…

Reason Subpotent Drug: confirmed subpotency in one lot of this product that was packaged and stored in syringes.

Pharmedium Services, LLC D-0093-2017