Exact FDA event identifier

Event 91672

13 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: February 09, 2023
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: L. Perrigo Company

Dossier provenance

Source snapshots represented here

openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

13 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 13

Allergy, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 72288-847-39), and b)150-count cartons (NDC 72288-847-47 and 72288-847-37), Distributed By: Amazon.com Services LLC., 410 Terry Avenue N., Seattle, WA 98109.

D-0900-2023

Recall number: D-0900-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 11,904 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot # a) 2GR0329, Exp. date 04/24 Lot # b) 2DR0472, Exp. date 02/23; 2MR0417, Exp. date 07/24

Distribution pattern

Nationwide within the USA

drug · product 2 of 13

Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 150-count cartons, Distributed By: BJ's Wholesale Club, 25 Research Drive, Westborough, MA 01581. NDC 68391-847-47

D-0901-2023

Recall number: D-0901-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 23,868 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #:2DV1863, 2HV2698, Exp. date 12/23; 2GV1583, Exp. date 02/24; 2GV1950, 2HV2697, Exp. Date 01/24.

Distribution pattern

Nationwide within the USA

drug · product 3 of 13

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons, Distributed By: Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

D-0902-2023

Recall number: D-0902-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 3,240 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: 2JE2185, Exp. date 01/24

Distribution pattern

Nationwide within the USA

drug · product 4 of 13

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39

D-0903-2023

Recall number: D-0903-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 16,200 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: 2DV1925, Exp. date 06/23

Distribution pattern

Nationwide within the USA

drug · product 5 of 13

aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Packaged For: Your Military Exchanges, By: Perrigo Company, Allegan, MI USA 49010. NDC 55301-847-39

D-0904-2023

Recall number: D-0904-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 1,920 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: 2ER0285,Exp. date 01/24

Distribution pattern

Nationwide within the USA

drug · product 6 of 13

Allergy ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg, 180-count cartons, Packaged by: Perrigo, 515 Eastern Ave., Allegan, MI 49010 USA. NDC 63981-847-48

D-0905-2023

Recall number: D-0905-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 360,184

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: 2DV1487, 2DV1870, 2DV1871, 2DV1873, 2EV1676, 2GV2132, 2HV2679, Exp. date 12/23; 2DV2000, exp. date 11/23; 2LV1573, 2MV1314, Exp. date 04/24; 2FV1764, 2FV1765 2FV1766, 2GV1579, 2GV1937, 2GV1941 , 2GV1942, 2GV2157, 2HV1886, 2HV1997, 2HV2019, 2HV2047, Exp. datev02/24; 2EV1666, 2EV1667, 2EV1668, 2EV1670, 2EV1671, 2EV1672, 2EV1674, 2EV1677, 2EV1678, 2HV2017, Exp. date 01/24.

Distribution pattern

Nationwide within the USA

drug · product 7 of 13

allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 79481-0847-0), b)30-count cartons (NDC 79481-0847-1), and c) 45-count cartons (NDC 79481-0847-2), Distributed by: MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.

D-0906-2023

Recall number: D-0906-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 59,688 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: a) 2JE1882, Exp. date 01/24 b) 2FV1918, 2ER0411, Exp. date 01/24; 2GV1902, Exp. date 04/24; 2CR0652, 2DR0465, Exp. date 12/23; 2GR0329, Exp. date 04/24 c)2CR0653, 2DR0466, Exp. date 12/23; 2ER0287, 2ER0412, Exp. date 01/24

Distribution pattern

Nationwide within the USA

drug · product 8 of 13

Fexofenadine Hydrochloride Tablets, 180 mg, 100-count cartons, Distributed by: Perrigo, Allegan, MI 49010. NDC 45802-847-78

D-0907-2023

Recall number: D-0907-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 15,504 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: 2DR0351, Exp. date 12/23

Distribution pattern

Nationwide within the USA

drug · product 9 of 13

Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons (NDC 0113-0847-95), Distributed by: Perrigo, Allegan, MI 49010.

D-0908-2023

Recall number: D-0908-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 32,376 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: a) 2DV1869, 2EV1613, 2EV1614, Exp. date 12/23; 2EV1820, 2FV1943, Exp. date 01/24; 2GV1893, Exp. date 04/24. Lot #: b) 2CR0653, 2DR0466, Exp. date 12/23, 2ER2087, Exp. date 01/24

Distribution pattern

Nationwide within the USA

drug · product 10 of 13

allergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)30-count cartons (NDC 56062-847-39); and b) 45-count cartons (NDC 56062-847-95), Distributed by: Publix Super Markets, Inc., 3300 Publix Corporate Parkway, Lakeland, FL 33811.

D-0909-2023

Recall number: D-0909-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 32,904 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: a) 2CR0652, 2DR0464, 2DR0465,Exp. Date 12/23; 2ER0285, Exp. Date 01/24. b) 2DR0466, Exp. Date 12/23; 2ER0412, Exp. Date 01/24; 2GR0330, Exp. Date 04/24

Distribution pattern

Nationwide within the USA

drug · product 11 of 13

allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-count cartons (NDC 11673-617-39), c)70-count cartons (NDC 11673-617-01), and d)150-count cartons (11673-617-47), Distributed by: Target Corporation, Minneapolis, MN 55403.

D-0910-2023

Recall number: D-0910-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 208,416 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: a) 2HE2032, 2JE1882, 2JE2185 Exp. Date 01/24; b) 2DR0464, 2ER0410, Exp. Date 12/23; 2ER0286, 2ER0411, Exp. Date 01/24 c) 2DR0467, 2DR0468, 2DR0469, 2ER0288, Exp. Date 12/23 d) 2ER0414, Exp. Date 01/24, 2GR0333, Exp. Date 02/24

Distribution pattern

Nationwide within the USA

drug · product 12 of 13

Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count cartons, Distributed by: Thirty Madison, Inc., New York, NY 10001. NDC 45 tablets: 80159-112-03

D-0911-2023

Recall number: D-0911-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 6,216 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot#: 2DR0471, Exp. Date 12/23

Distribution pattern

Nationwide within the USA

drug · product 13 of 13

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-count cartons (NDC 36800-691-95), and 90-count cartons (NDC 36800-691-75), Distributed by: Topco Associates LLC, Elk Grove Village, IL 60007.

D-0912-2023

Recall number: D-0912-2023
Initiated: February 09, 2023
Classification: Class II
Status: Terminated
Recalling firm: L. Perrigo Company
Quantity: 44,280 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurities/Degradation Specifications

Code information

Lot #: a) 2FV1948, 2ER0285, 2ER0411, Exp. Date 01/24 b)2CR0653, Exp. Date 12/23 c)2GR0331, Exp. Date 04/24

Distribution pattern

Nationwide within the USA