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Showing 14261–14280 of 14360 results

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Dextrose Injection (Hospira) – sterility leak (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Sodium Chloride Injection (Hospira) – sterility leak (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Sodium Chloride Irrigation (Hospira) – Possible Leaking Bags (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Dextrose Injection (Hospira) – Possible Leaking Bags (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Sodium Chloride Injection (Hospira) – sterility leak (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Glycine Irrigation (Hospira) – sterility leak (2012)

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Class IIModerate

FDAMay 4, 2012Nationwide• Hospira Inc.

Zeosa Birth Control (Teva) – impurity specifications (2012)

Impurities/Degradation: This recall is being carried out due to the potential for some lots not meeting impurity specifications.

Class IIModerate

FDAMay 2, 2012Nationwide• Teva Pharmaceuticals USA, Inc.

Octreotide Acetate Injection (Ben Venue) – short fill (2012)

Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.

Class IIModerate

FDAMay 1, 2012Nationwide• Ben Venue Laboratories Inc

Midazolam HCl Injection (Ben Venue) – short fill (2012)

Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.

Class IIModerate

FDAMay 1, 2012Nationwide• Ben Venue Laboratories Inc

Dorzolamide HCI/Timolol Maleate Solution (Apotex) – particulate matter (2012)

Presence of Particulate Matter: Lots identified in this recall notification may contain small particulates.

Class IIModerate

FDAApr 30, 2012Nationwide• Apotex Inc.

Midol Complete Gelcaps (Bayer) – label mix-up (2012)

Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken within a 24-hour period, does not match the statement on the carton.

FDAApr 26, 2012Nationwide• Bayer Healthcare, LLC

Midol Complete Caplets (Bayer) – label mix-up (2012)

Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken within a 24-hour period, does not match the statement on the carton.

FDAApr 26, 2012Nationwide• Bayer Healthcare, LLC

Cabergoline Tablets (Teva) – impurity specification (2012)

Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life

FDAApr 24, 2012Nationwide• Teva Pharmaceuticals USA, Inc.

Epinephrine Injection (Luitpold) – particulate matter (2012)

Presence of Particulate Matter

Class IIModerate

FDAApr 24, 2012Nationwide• Luitpold Pharmaceuticals, Inc.

Jolessa Tablets (Teva) – contraceptive sequence issue (2012)

Contraceptive Tablets Out of Sequence: This recall has been initiated due to the potential that some regimen packages may not contain placebo tablets.

FDAApr 23, 2012Nationwide• Teva Pharmaceuticals USA, Inc.

X-Rock Supplement (XRock) – unapproved ingredients (2012)

Marketed Without an Approved NDA/ANDA: product tested positive for PDE-5 Sildenafil and PDE-5 Hydroxythiohomosildenafil. Hydroxythiohomosildenafil is an analog of sildenafil, an FDA approved prescription drug for Erectile Dysfunction (ED).

FDAApr 21, 2012Nationwide• XRock Industries, LLC

Loxitane Capsules 10mg (Watson) – Outdated Package Insert (2012)

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

FDAApr 17, 2012Nationwide• Watson Laboratories Inc

Loxapine Capsules 5mg (Watson) – Outdated Package Insert (2012)

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

FDAApr 17, 2012Nationwide• Watson Laboratories Inc

Loxapine Capsules 50mg (Watson) – Outdated Package Insert (2012)

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

FDAApr 17, 2012Nationwide• Watson Laboratories Inc

Loxapine Capsules 25mg (Watson) – Outdated Package Insert (2012)

Labeling: Incorrect or Missing Package Insert: An outdated version of a patient outsert was used when packaged.

FDAApr 17, 2012Nationwide• Watson Laboratories Inc

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