Lupin Mibelas 24 Fe recall — FDA D-1093-2017
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Complete FDA and NHTSA recall records dated in 2017, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.
Subpotent Drug: products are labeled as having SPF 10 protection; however, this claim cannot be 100% guaranteed.
Failed Impurities/Degradation Specification: single unknown impurity OOS 0.33% (Limit:NMT 0.20%W/W) at the three month stability point.
Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies…
The reason for recall was that some jars of Publix GreenWise Cashew Butter may actually contain Almond Butter.
McCain Foods Canada, Inc. initiated a voluntary recall of their frozen MCCAIN ONION RING BATTERED PORTION PERFECT ¿ 60X4 oz following a supplier's recall of a raw ingredient due to…
Sunneel Health Foods received a call from their customer indicating some of their Vegan Match Cocoa Parfaits were misbranded as PB & J Parfaits. The ingredient statement failed to declare…
Presence of Particulate Matter: Silicone oil
Failed Moisture Limits: out of specification test results for water content obtained during stability testing.
Firm received notification that a consumer found a peanut in NatureBox Sticks 'n Stones snack mix that contains Cashews and Almonds, not peanuts.
Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
General Mills was notified by customer of IQF noodles found in IQF rice. The IQF noodles contain eggs and wheat.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Thai Shrimp Salad has incorrect back label showing information for Chicken Florentine Salad
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.
Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is recalled because label declared butter, cream, or dairy but milk is NOT declared.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.