Your safety is our #1 priority. From time to time, certain prescription medications dispensed by Kinney Drugs may be recalled by the manufacturer(s). When this happens, we will display details on the recall(s), along with any instructions provided by the manufacturer(s) .
MARCH 15th, 2023 -
Event Description:
Sandoz is voluntarily recalling the above items/lots due to the packaging of these lot numbers is not child-resistant as required by the Poison Prevention Packaging Act. This recall is to the Consumer level.
*Examine your inventory for the affected item completely and stop dispensing and distributing the lots immediately. Quarantine any product from these lots that remain in inventory until further notice.
Consumer Information:
Continue using the medication as directed by your physician. Due to risk of harm to children, immediately secure the medication out of the sight and reach of children. To order a free child-resistant, resealable pouch in which to store your medication, call 1-866-300-2207 Monday-Friday, 8am-5pm ET.
MARCH 3rd, 2023 -
Actions to be taken by the Customer:
Immediately discontinue using affected lot numbers.
Consumers can call Inmar at 855-275-1273 and a product return kit and prepaid shipping label will be sent to you for product return of affected lots.
FEBRUARY 3RD, 2023 -
IBSA is voluntarily recalling the above items/lots because these lots may be subpotent. THe company's analyses show a slight decrease below 95.0% of its labeled amount in levothyroxine sodium (T4) for some lots. This recall is to the Consumer level. Affected product started shipping August 2, 2022.
For more information, please click here.
DECEMBER 21ST, 2022 -
DECEMBER 6TH, 2022 -
| SKU | Description | UPC | LOT # | Exp Date |
| 0016108 | ADVIL EZ 200CT TAB. | 30573015421 | 953D | 5/31/2025 |
| 0037776 | ADVIL MINI 200 CT LGEL | 30573176913 | R93517 | 2/29/2024 |
| R94072 | 2/29/2024 | |||
| R94073 | 2/29/2024 | |||
| T00655 | 3/31/2025 |
Advil is voluntarily recalling the above products due to an issue causing the “peel back” labels on the bottle to possibly not function correctly, and certain information in the drug facts panel may be unreadable upon opening the label:
AUGUST 8TH, 2022 -
| Description | Lot # and Exp Date | NDC | UPC | Econo # |
| MAGNES CITR LIQ MMP 296ML | 0533216 05/31/23; 0518463 01/31/23; 0518464 01/31/23; 0518465 12/31/22; 0518467 01/31/23; 0518468 01/31/23; 0528485 04/30/23; 0528486 03/31/23; 0498815 08/31/22; 0530048 04/30/23; 0518460 12/31/22; 0533217 05/31/23; 0534876 06/30/23; 0537774 06/30/23; 0537775 06/30/23; 0537776 06/30/23; 0537777 06/30/23; 0537779 06/30/23; 0528488 04/30/23; 0508944 11/30/22; 0498819 08/31/22; 0501884 09/30/22; 0501885 09/30/22; 0501886 09/30/22; 0501887 09/30/22; 0501888 09/30/22; 0505247 10/31/22; 0518462 12/31/22; 0505249 10/31/22; 0518461 12/31/22; 0508953 11/30/22; 0508955 11/30/22; 0508956 11/30/22; 0508957 11/30/22; 0508959 11/30/22; 0511721 12/31/22; 0511723 12/31/22; 0537782 06/30/23; 0505248 10/31/22; 0563518 03/31/24; 0537780 06/30/23; 0551969 11/30/23; 0551970 11/30/23; 0556094 12/31/23; 0556817 12/31/23; 0558192 01/31/24; 0562244 02/29/24; 0551895 10/31/23; 0562309 03/31/24; 0542940R2 09/30/23; 0563520 03/31/24; 0563595 04/30/24; 0564023 03/31/24; 0567126 05/30/24; 0568829 04/30/24; 0569326 05/30/24; 0570583 06/30/24; 0570584 06/30/24; 0562306 03/31/24; 0542936 09/30/23; 0572458 06/30/24; 0537783 06/30/23; 0539834 08/31/23; 0539835 07/31/23; 0539835R2 07/31/23; 0539836 08/31/23; 0542935 09/30/23; 0551968 11/30/23; 0542935R2 09/30/23; 0537781 06/30/23; 0542936R1 09/30/23; 0542937 09/30/23; 0542937R1 09/30/23; 0542938 09/30/23; 0542938R1 09/30/23; 0542939 09/30/23; 0542939R1 09/30/23; 0542940 09/30/23; 0542935R1 09/30/23 | 00904678744 | 30904678744 | 3591252 |
Major Pharmaceuticals has been notified by Vi-Jon, Inc. that they are voluntarily recalling the above item/lots due to testing showing that certain lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor exceed the limit for Aerobic Plate County & Yeast and Mold (identified as Gluconacetobacter liquefaciens). This recall is to the consumer level.
Consumer Information:
If you have questions regarding this recall, contact 1-8---943-2387.
JULY 12TH, 2022 -
| NDC | Description | UPC | Batch # | Exp Date |
| 49502-394-75 | INSULIN GLARGINE (INSULIN GLARGINE-YFGN) INJECTION, 100 UNITS/ML (U-100) | 3 mL Prefilled Pen | 16345 | 01/31/2024 |
Mylan Pharmaceuticals Inc (a Viatris company) is conducting a voluntary recall at the consumer level of one batch, BF21002895, of Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), 3mL prefilled pens, which are packaged in cartons of 5 pens. The product is not the branded Semglee pen but the unbranded Insulin Glargine-yfgn pens. This batch is being recalled due to the potential for the label to be missing on some pens.
For patients receiving treatment with more than one type of insulin (e.g., both short and long-acting insulin), a missing label on Insulin Glargine pens could lead to a mix-up of products/strengths, which may result in less optimal glycemic control (either high or low blood sugar) which could result in serious complications.
Consumer Information:
Contact Sedgwick at 1-877-643-8438 for the documentation packet to return the unlabeled product.
APRIL 29TH, 2022 -
Consumer Information:
Consumers should contact their physician for further medical advice. If you have the affected lot number(s) or if you are unsure, please contact Qualanex at 888-504-2012 for assistance.
APRIL 27TH, 2022 -
APRIL 19TH, 2022 -
