FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Albertsons Inc
- Product
- Broccoli Carrots Cauliflower with Ranch Dip 330 cal, 9 oz..…
- Reason
- Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Colorado, Nebraska, Northwestern New Mex…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Albertsons Inc
- Product
- Vegetables Steaming, 13 oz.. UPC 24214000000 Sold in Alb…
- Reason
- Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Colorado, Nebraska, Northwestern New Mex…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Albertsons Inc
- Product
- Premium Vegetable Tray, 2 lb. 14 oz.. UPC 24210800000 So…
- Reason
- Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Colorado, Nebraska, Northwestern New Mex…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Albertsons Inc
- Product
- Veggies w/ Dip, 8 oz. UPC 24201200000 Sold in Albertson'…
- Reason
- Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Colorado, Nebraska, Northwestern New Mex…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Albertsons Inc
- Product
- Cauliflower Chopped, 8 oz. UPC 24105000000 Sold in Alber…
- Reason
- Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Colorado, Nebraska, Northwestern New Mex…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- COLORADO COLESLAW Ingredients: Salad Dressing, Cabbage, Toma…
- Reason
- The firm was notified that the products may be contaminated with Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Product was shipped to: CO, NM, UT & WY.
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- California Broccoli Salad Kit Ingredients: Salad Dressing, C…
- Reason
- The firm was notified that the products may be contaminated with Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Product was shipped to: CO, NM, UT & WY.
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- BROCCOLI ALMOND SALAD Ingredients: Broccoli, Dressing, Grape…
- Reason
- The firm was notified that the products may be contaminated with Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Product was shipped to: CO, NM, UT & WY.
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- ASIAN PASTA SALAD Ingredients: Cooked Pasta, Broccoli, Green…
- Reason
- The firm was notified that the products may be contaminated with Listeria monocytogenes.
- Published
- November 15, 2017
- Distribution
- Product was shipped to: CO, NM, UT & WY.
View recall →
FDA Recall
Terminated
Historical recordClass II
Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA.
by Teva Pharmaceuticals USA
- Reason
- Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe, (50 mg / 5 mL Total Dose) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-850-09
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag, Each bag contains 9.3 mEq Ca++ Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0510-30
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride 10 mL Fill Volume in a Single Dose Syringe (1,000 mcg / 10 ml Total Dose), Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR, NDC 70004-0810-12
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 mL in Single Dose CADD Cassette (Total morphine Dose 100 mg per 100 mL) (NDC 70004-0100-63) b) Total Volume 50 mL in Single Dose Syringe (Total morphine Dose 50 mg / 50 mL) (NDC 70004-0100-22) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl Dose (200 mcg per 100 mL) in 0.9% Sodium Chloride single dose CADD Cassette Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0264-64
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% (Total FentaNYL Dose 500 mcg/250 mL) in 0.9% Sodium Chloride 250 mL Bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205. NDC 70004-0231-40
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29
by SCA Pharmaceuticals, LLC
- Reason
- Lack Of Assurance Of Sterility.
- Published
- November 8, 2017
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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